{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/blue-bell-icon/"},"x-facet":{"type":"city","slug":"blue-bell-icon","display":"Blue Bell Icon","count":28},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8b070b2c-2d3"},"title":"Manager, FSA","description":"<p>As a Manager, Feasibility and Site Activation (FSA) at ICON, you will lead teams responsible for delivering high-quality feasibility assessments and efficient site activation for global clinical trials.</p>\n<p>Your focus will be on coordinating site start-up and activation delivery, resolving issues, and developing team capability. Key responsibilities include:</p>\n<ul>\n<li>Managing FSA project teams to deliver country and site feasibility, start-up strategies, and activation activities in line with timelines and quality expectations.</li>\n<li>Accountable for resourcing, utilization, forecasting and headcount control, to ensure staffing levels are conducive to operational and financial success.</li>\n<li>Overseeing the coordination of essential documents, regulatory and ethics submissions, and contract/start-up packages for assigned studies.</li>\n<li>Reviewing feasibility data, assumptions, and risks, and partnering with stakeholders to develop mitigation plans and realistic start-up forecasts.</li>\n<li>Collaborating with business development and operational teams to support proposals, bid defences, and customer meetings with robust FSA input.</li>\n<li>Monitoring performance metrics for feasibility and site activation, identifying trends and driving continuous improvement initiatives.</li>\n<li>Providing coaching, feedback, and development opportunities to FSA staff, fostering a culture of accountability and collaboration.</li>\n</ul>\n<p>You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in life sciences, healthcare, business, or a related field, or equivalent experience.</li>\n<li>Significant experience in clinical research with a strong focus on feasibility, site selection, and study start-up.</li>\n<li>Proven ability to manage projects or teams in a fast-paced, matrixed environment.</li>\n<li>Strong analytical and planning skills, with experience interpreting feasibility data and operational metrics.</li>\n<li>Excellent communication and stakeholder management skills, including customer-facing experience.</li>\n<li>Continuous improvement mindset, with a focus on quality, predictability, and operational excellence.</li>\n<li>Willingness to travel as required (minimal).</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Manager--FSA--Feasibility-Site-Activation-_JR160277","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Manager--FSA--Feasibility-Site-Activation-_JR160277","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","feasibility","site selection","study start-up","project management","analytical skills","communication skills","stakeholder management"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-27T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical research, feasibility, site selection, study start-up, project management, analytical skills, communication skills, stakeholder management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9ea9f9b6-90e"},"title":"Clinical Study Manager","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As a Clinical Study Manager at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. Key responsibilities include:</p>\n<ul>\n<li>Overseeing the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.</li>\n<li>Collaborating with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.</li>\n<li>Developing and managing study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.</li>\n<li>Leading the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.</li>\n<li>Ensuring data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.</li>\n<li>Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.</li>\n<li>Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.</li>\n<li>Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Study-Manager_JR161860","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic Solutions","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Study-Manager_JR161860","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial management","regulatory requirements","project management","communication skills","data analysis"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-07T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial management, regulatory requirements, project management, communication skills, data analysis"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_825f6cef-512"},"title":"Lead Clinical Research Associate - 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An advanced degree is preferred.</li>\n<li>8+ years monitoring Oncology (solid tumor) trials (with a minimum of 4 years monitoring phase I and/or Phase III Oncology) is required.</li>\n<li>Previous experience independently conducting on-site and remote monitoring visits (site qualification, initiation, monitoring, and close-out) is required.</li>\n<li>Experience utilizing Veeva CTMS and TMF is required.</li>\n<li>Experience supporting site and/or sponsor inspections is preferred.</li>\n<li>Experience auditing sites and TMF are preferred.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Lead-CRA--Principal-CRA_JR160760","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic Solutions","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Lead-CRA--Principal-CRA_JR160760","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Veeva CTMS","TMF","GCP","clinical trial regulations","Oncology trials"],"x-skills-preferred":["auditing sites","supporting site inspections"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-29T21:36:06.785Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Veeva CTMS, TMF, GCP, clinical trial regulations, Oncology trials, auditing sites, supporting site inspections"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_2af03e9a-930"},"title":"Feasibility Informatics Manager","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Feasibility Informatics Manager, you will serve as a technical feasibility strategy expert, leading and managing the process of clinical project feasibility in support of proposal teams by assisting Business Development with the generation of cost proposals, providing input and advice relating to operational strategy, and supporting client interactions and long-term strategic partnerships.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Recognize, exemplify, and adhere to ICON&#39;s values (Collaboration, Integrity, Inclusion, and Agility) which center around our commitment to people, clients, and performance.</li>\n<li>Create a culture of process improvement with a focus on streamlining our processes, adding value to our business and meeting client needs.</li>\n<li>Travel (approximately 20%) domestic and/or international as needed.</li>\n<li>Maintain communication and relationships between all relevant parties to ensure that available intelligence is utilized to deliver optimal, data-driven feasibility strategy solutions.</li>\n<li>Prepare feasibility data by collecting data from data assets, determining site profiles, developing feasibility strategies, and providing full documentation in proposals.</li>\n<li>Conduct evidence-based feasibility by establishing viability of proposed projects through interrogation of internal and external performance metrics and resources.</li>\n<li>Perform accurate and correct data analysis and interpretation to support feasibility strategy solutions.</li>\n<li>Support and/or present strategic project planning during bid defense meetings.</li>\n<li>Initiate, conduct, coordinate, analyze, and report feasibility studies as contracted on time and on budget.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Master&#39;s Degree</li>\n<li>6-9 years of experience in a Clinical Research environment</li>\n</ul>\n<p><strong>Rewards &amp; 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You will provide senior medical, scientific and radiological expertise to support imaging strategy, clinical trial delivery, independent reader oversight, business development and client engagement.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Provide senior medical and radiology leadership for sponsor studies, including imaging strategy, protocol design, imaging manuals, read methodology, charters, system requirements, training materials, quality control and independent reviewer processes.</li>\n<li>Partner with Business Development and operational teams to support new business opportunities, bid defenses, capabilities meetings and client relationship development through expert medical and scientific input.</li>\n<li>Represent ICON&#39;s medical, scientific and imaging expertise in internal and external discussions, making independent recommendations that support study quality, regulatory readiness and client success.</li>\n<li>Support responses to requests for proposals and information by providing scientific, medical and technical input that demonstrates ICON&#39;s imaging expertise in clinical trials.</li>\n<li>Provide real-time consultation to internal teams, sponsors, sites and clients on imaging-related scientific and operational questions.</li>\n<li>Build trusted client relationships by advising on imaging strategy, discussing and resolving study-specific imaging issues, and supporting responses to regulatory authority queries related to study design and radiological assessment.</li>\n<li>Supervise independent read teams, including reader training, ongoing Q&amp;A, performance monitoring, assessment of inter-reader variability, retraining plans and oversight of read quality.</li>\n<li>Oversee imaging reads and provide medical review and guidance to ensure read outputs are clinically appropriate, scientifically sound and aligned with study requirements.</li>\n<li>Contribute to ICON&#39;s scientific credibility through participation in industry forums, imaging standardization initiatives, scientific meetings and external presentations.</li>\n<li>Mentor medical, scientific and operational colleagues to strengthen understanding of imaging endpoints, clinical trial objectives and the role of a CRO in drug development.</li>\n<li>Lead, motivate and advise project and study teams to deliver high-quality imaging and medical/scientific deliverables for clients.</li>\n<li>Guide medical and scientific activities to ensure timely, complete and client-focused delivery across assigned studies and programs.</li>\n<li>Develop capability across medical, scientific and operations teams by translating complex clinical, radiological and drug development concepts into practical study guidance.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>MD with fellowship training in radiology is required; additional training or demonstrated experience supporting clinical research is strongly preferred.</li>\n<li>Expertise in neuroradiology and body imaging is strongly preferred.</li>\n<li>Cross-certification in nuclear medicine is preferred.</li>\n<li>Deep expertise in imaging endpoints for clinical trials, with comprehensive knowledge of drug development, biomarker development, adaptive design, regulatory submission and post-marketing studies.</li>\n<li>Strong working knowledge of applicable regulatory expectations, including ICH-GCP and relevant regional requirements.</li>\n<li>Demonstrated ability to lead complex, large-scale projects and influence through scientific credibility, sound judgment and effective stakeholder engagement.</li>\n<li>Excellent communication and presentation skills, with the ability to advise clients, support business development activities and represent ICON in public or scientific forums.</li>\n<li>Live in the US, UK, or Ireland</li>\n<li>Ability to travel up to 10%</li>\n</ul>\n<p><strong>Rewards &amp; 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Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. 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In this strategic leadership role, you will provide scientific and clinical imaging expertise across business development, project delivery, and innovation initiatives.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Provide scientific and medical imaging expertise to Commercial Development, Operations, and project teams throughout the clinical trial lifecycle.</li>\n<li>Serve as a scientific subject matter expert and trusted advisor for sponsors, supporting study design, protocol review, imaging endpoint strategy, and solution development.</li>\n<li>Provide scientific leadership and strategic guidance for imaging components of clinical trials focused on MASH, obesity, diabetes, and other metabolic diseases.</li>\n<li>Advise sponsors and internal teams on the application of imaging biomarkers, quantitative imaging methods, and emerging technologies relevant to metabolic disease research.</li>\n<li>Review and provide scientific oversight for imaging charters, image review manuals, site-facing materials, sponsor deliverables, and study reports.</li>\n<li>Ensure imaging methodologies, endpoints, and operational approaches are aligned with protocol objectives, regulatory expectations, and industry best practices.</li>\n<li>Contribute to the advancement of imaging methodologies and endpoint strategies that support the assessment of metabolic disease progression, treatment response, and clinical outcomes.</li>\n<li>Support business development activities by participating in client meetings, capabilities presentations, bid defense meetings, RFPs, RFIs, and proposal development.</li>\n<li>Build and maintain strong relationships with sponsors and key stakeholders, providing scientific consultation throughout the sales and study execution process.</li>\n<li>Represent ICON at scientific conferences, industry forums, and working groups through presentations, publications, and participation in imaging standardization initiatives.</li>\n<li>Partner with Marketing and Commercial teams to communicate ICON&#39;s scientific differentiators and support thought leadership activities.</li>\n<li>Provide scientific training, mentorship, and consultation to internal teams, fostering continued development of imaging expertise across the organization.</li>\n<li>Collaborate with Product Development and Technology teams to define scientific requirements and support the enhancement of innovative imaging solutions and proprietary software platforms.</li>\n<li>Stay informed of emerging scientific, clinical, and regulatory developments related to metabolic diseases and their associated imaging applications.</li>\n<li>Travel domestically and internationally as required (approximately 10%).</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>PhD required in a relevant scientific or technical discipline, preferably Biomedical Engineering, Electrical Engineering, Medical Physics, Physics, Imaging Sciences, or a closely related quantitative imaging field.</li>\n<li>Significant experience within the pharmaceutical, biotechnology, CRO, or clinical research industry supporting imaging components of clinical trials.</li>\n<li>Direct experience supporting imaging studies and imaging biomarkers in MASH, obesity, diabetes, and other metabolic disease indications is required.</li>\n<li>Deep understanding of imaging biomarker development, quantitative image analysis, imaging endpoint strategy, and clinical trial design.</li>\n<li>Experience in applying advanced imaging technologies, image analysis methodologies, and emerging imaging techniques in metabolic disease research.</li>\n<li>Demonstrated expertise in imaging modalities commonly utilized in metabolic disease clinical trials, including the assessment of liver fat, fibrosis, body composition, and related metabolic endpoints.</li>\n<li>Experience supporting business development activities, including client interactions, scientific consultation, proposal development, and bid defense meetings.</li>\n<li>Strong leadership and collaboration skills with the ability to influence and work effectively across global, cross-functional teams.</li>\n<li>Excellent scientific communication, presentation, and stakeholder management capabilities.</li>\n<li>Demonstrated ability to translate complex scientific concepts into practical, client-focused solutions.</li>\n<li>Strong strategic thinking, problem-solving, and decision-making skills.</li>\n<li>Commitment to quality, innovation, and delivering exceptional customer experiences.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Director--Medical---Scientific-Affairs---Metabolic-Disease-Imaging_JR158659","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Director--Medical---Scientific-Affairs---Metabolic-Disease-Imaging_JR158659","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Biomedical Engineering","Electrical Engineering","Medical Physics","Physics","Imaging Sciences","MASH","obesity","diabetes","metabolic disease research"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Biomedical Engineering, Electrical Engineering, Medical Physics, Physics, Imaging Sciences, MASH, obesity, diabetes, metabolic disease research"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1e8abe25-fa2"},"title":"Senior Clinical Trial Manager","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. Key responsibilities include:</p>\n<ul>\n<li>Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation.</li>\n<li>Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.</li>\n<li>Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.</li>\n<li>Timely Study Start-Up &amp; Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.</li>\n<li>Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary.</li>\n<li>Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.</li>\n<li>Bachelor&#39;s degree in health, life sciences, or other relevant fields of study.</li>\n<li>At least 10+ years of relevant experience in clinical trial management.</li>\n<li>Preferred: 2+ years of monitoring experience.</li>\n<li>Experience in managing complex or global trials is advantageous.</li>\n<li>Preferred: Experience in managing all trial components from start-up to database lock.</li>\n<li>Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.</li>\n<li>Willingness to travel as required (approximately 25%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Trial-Manager_JR163000","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Trial-Manager_JR163000","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Clinical Trial Management","Budget Oversight","Study Oversight","Performance Optimization","Enrollment Management","Study Integrity"],"x-skills-preferred":["Monitoring Experience","Complex or Global Trials Management","Coaching/Mentoring","Team Leadership"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-22T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Trial Management, Budget Oversight, Study Oversight, Performance Optimization, Enrollment Management, Study Integrity, Monitoring Experience, Complex or Global Trials Management, Coaching/Mentoring, Team Leadership"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_5433adf1-eaf"},"title":"Sr. CRA - Phase 1 Oncology West Coast","description":"<p>As a Senior CRA at ICON Strategic Solutions, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. This position is sponsor dedicated and supporting Phase I Oncology trials.</p>\n<p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:</p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Willingness to travel as required (approximately 60%)</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Research-Associate_JR160829","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic Solutions","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Research-Associate_JR160829","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$110,520.00-$138,150.00","x-skills-required":["Clinical trial monitoring","Good Clinical Practice (GCP)","Regulatory requirements","Data integrity","Site management"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-23T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical trial monitoring, Good Clinical Practice (GCP), Regulatory requirements, Data integrity, Site management","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":110520,"maxValue":138150,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_268714bb-edd"},"title":"Clinical Research Associate","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As a Clinical Research Associate (CRA II) at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 2 years of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Willingness to travel as required (approximately 60%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/CRA-2_JR157374","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic Solutions","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/CRA-2_JR157374","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial monitoring","data analysis","ICH-GCP guidelines","communication skills","organisational 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environment.</li>\n<li>Proven ability to manage multiple priorities, stakeholders, and deadlines simultaneously.</li>\n<li>Strong project planning, organization, and execution skills.</li>\n<li>Excellent communication, facilitation, presentation, and stakeholder management abilities.</li>\n<li>Experience driving initiatives through influence rather than direct authority.</li>\n<li>Demonstrated ability to identify risks, solve problems, and deliver results in dynamic environments.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong> ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Director--Account-Management---Partnership-Build---Optimization_JR161520","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Director--Account-Management---Partnership-Build---Optimization_JR161520","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Project planning","Communication","Facilitation","Presentation","Stakeholder management","Problem-solving","Risk 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Sr-Manager--Clinical-Operations---Imaging_JR160066","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Sr-Manager--Clinical-Operations---Imaging_JR160066","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","medical imaging","healthcare operations","leadership","quality management"],"x-skills-preferred":["advanced degree","relevant leadership certifications","experience leading geographically dispersed 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Manager--Project-Management---Imaging_JR152743-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Manager--Project-Management---Imaging_JR152743-1","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["project management","leadership","communication","analytical skills"],"x-skills-preferred":["PMP certification","life sciences","business administration"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-21T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"project management, leadership, communication, analytical skills, PMP certification, life sciences, business administration"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_eea4c7d6-71f"},"title":"Executive Director, Deals Center of Excellence","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>The Executive Director, Deal Center of Excellence leads a focused global commercial capability that improves ICON&#39;s approach to winning, structuring, negotiating, and expanding its most strategic customer partnerships across the pharmaceutical, biotechnology, and medical device sectors.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Define and lead the global Deal Centre of Excellence strategy, operating model, governance, performance measures, and implementation.</li>\n<li>Prioritize and support strategically important pursuits, preferred-provider opportunities, complex renewals, and other major deals.</li>\n<li>Lead structured pursuit strategy workshops that establish customer objectives, win themes, stakeholder plans, competitive positioning, risks, investment choices, negotiation goals, and clear ownership across the deal team.</li>\n<li>Shape commercial solutions and partnership structures that balance customer value, competitive positioning, operational feasibility, pricing discipline, risk, and sustainable economics.</li>\n<li>Direct executive deal reviews by presenting evidence-based recommendations on probability of success, strategic value, commercial options, required investments, key risks, and negotiation guardrails.</li>\n<li>Partner closely with Commercial Finance to ensure that commercial strategy is robust while financial governance and control responsibilities remain independent and effective.</li>\n<li>Lead negotiation of identified strategic pursuits in collaboration with business development, operations, and commercial finance.</li>\n<li>Build and maintain reusable playbooks, customer and competitor insights, win-loss learning, deal benchmarks, negotiation approaches, and post-award reviews to improve future pursuits and commercial capability.</li>\n<li>Develop a high-performing specialist team and influence broader commercial, operational, proposal, and leadership communities through coaching, training, 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Executive-Director--Deals-Center-of-Excellence_JR162116-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Executive-Director--Deals-Center-of-Excellence_JR162116-1","x-work-arrangement":"remote","x-experience-level":"executive","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Business","Finance","Economics","Life Sciences","Commercial Strategy","Deal Management","Negotiation","Financial Modeling","Pricing 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CTMs.</li>\n</ul>\n<p><strong>You are:</strong></p>\n<ul>\n<li>A graduate with a Bachelor&#39;s degree in Life Sciences or equivalent, or a qualified RN.</li>\n<li>Eligible to work in United States without visa sponsorship.</li>\n<li>A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry.</li>\n<li>Experienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas.</li>\n<li>Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF.</li>\n<li>A clear communicator, problem-solver, and collaborative team player.</li>\n<li>Willing and able to travel up to 60% for on-site monitoring visits; preference given to candidates residing near major HUB airports to support efficient regional travel.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR155119","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic 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CTMS, eTMF, Life Sciences, clinical research"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_45f579d6-a59"},"title":"Clinical Project Manager (CNS/Rare Disease) - Remote, US","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Clinical Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Developing and managing detailed clinical project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.</li>\n<li>Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Project-Manager--CNS-Rare-Disease-_JR154464-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Project-Manager--CNS-Rare-Disease-_JR154464-1","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical project management","life science","project management","business","communication","interpersonal skills","CNS/Rare Disease"],"x-skills-preferred":["CRO","Biotech"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is 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working, and adoption of innovative technologies to improve efficiency and predictability of delivery.</li>\n<li>Provide effective portfolio governance and strategic oversight, supporting strong customer relationships, financial health, achievement of business objectives, and sustainable portfolio growth.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Significant leadership experience within clinical research, clinical development, or a related life sciences environment, with responsibility for complex global programs or portfolios.</li>\n<li>Strong knowledge of clinical trial startup activities, including site activation, regulatory processes, contracting, and associated operational dependencies.</li>\n<li>Demonstrated experience leading and developing people leaders and building high-performing teams within a complex, matrixed organization.</li>\n<li>Proven ability to manage portfolio performance across operational delivery, quality, financial performance, resource 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You are detail-oriented, collaborative, and capable of managing multiple priorities in a fast-paced environment.</p>\n<p><strong>Required Qualifications and Experience:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in business, life sciences, public health, communications, or a related discipline.</li>\n<li>Previous experience in proposal development, business development support, project coordination, or a related function within the pharmaceutical, healthcare, CRO, or clinical research industry.</li>\n<li>Experience developing proposals and responding to RFPs for Late Phase, Real World Evidence (RWE), observational, registry, post-marketing, or non-interventional studies strongly preferred.</li>\n<li>Understanding of clinical research methodologies, including Phase IV studies, prospective and retrospective observational research, patient registries, and real-world data collection approaches.</li>\n<li>Experience collaborating with cross-functional teams to develop client-focused proposals, budgets, and supporting documentation.</li>\n<li>Strong attention to detail and organizational skills with the ability to manage multiple proposal opportunities simultaneously under competing deadlines.</li>\n<li>Excellent written and verbal communication skills with the ability to effectively convey complex scientific and operational information.</li>\n<li>Proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint.</li>\n<li>Willingness to travel as required (approximately 5%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong> ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Proposals-Development-Associate-II_JR162525","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Proposals-Development-Associate-II_JR162525","x-work-arrangement":"remote","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["proposal development","clinical research","Microsoft Office","communication","project coordination"],"x-skills-preferred":["Late Phase research","Real World Evidence (RWE)","observational studies","registry studies","post-marketing studies","non-interventional studies"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-19T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"proposal development, clinical research, Microsoft Office, communication, project coordination, Late Phase research, Real World Evidence (RWE), observational studies, registry studies, post-marketing studies, non-interventional studies"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_60645e8d-731"},"title":"CRA II or Senior CRA","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. 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pathways.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-CRA_JR158562","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-CRA_JR158562","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial processes","ICH-GCP guidelines","organisational skills","communication skills"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-26T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial processes, ICH-GCP guidelines, organisational skills, communication skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_0a0b2aca-6cb"},"title":"Senior Site Selection Specialist - US - remote","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Site Selection Specialist, you will contact and build relationships with study investigators/sites and networks in assigned areas for the conduct of feasibility and potential 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with the site is tracked and data-based appropriately</li>\n<li>Support other team members on how to get the best information from sites</li>\n<li>Identify high-performing sites and develop relationships with them</li>\n<li>Deliver high-quality standards and strive for excellence</li>\n<li>Establish good relationships internally and externally</li>\n<li>Undertake other reasonably related duties as may be assigned from time to time</li>\n<li>Recognize, exemplify and adhere to ICON&#39;s values</li>\n<li>Embrace and contribute to our culture of process improvement with a focus on accelerating concept to cure</li>\n<li>Travel approximately 10% domestic and/or international, as required</li>\n<li>Implement the project-specific Site Selection strategy at the country level</li>\n</ul>\n<p><strong>What you need:</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree</li>\n<li>3-6 years of experience in a Clinical Research environment</li>\n<li>Good communication skills</li>\n<li>Good judgment and decision-making</li>\n<li>Proficient computer knowledge</li>\n<li>Proficiency in English language is mandatory</li>\n</ul>\n<p><strong>Benefits of Working in ICON:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Site-Selection-Specialist_JR157434","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Site-Selection-Specialist_JR157434","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":null,"x-salary-range":null,"x-skills-required":["Clinical Research","Communication","Judgment and Decision Making","Computer Knowledge","English Language"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental","bonus"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in 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As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>We are currently seeking a Talent Sourcing Recruiter - Contract to join our diverse and dynamic team. As a Talent Sourcing Recruiter at ICON, you will focus on building strong talent pipelines for critical roles, proactively identifying and engaging candidates to support ICON’s growth.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Focus on sourcing and hunting for talent</li>\n<li>Responsible for the successful sourcing of external candidates to support internal job requirements in the United States and Canada</li>\n<li>Develop external networks through web-based portals</li>\n<li>Fully utilize and maintain candidate databases and systems</li>\n<li>Work with the Talent Acquisition Business Partner’s to develop business and staffing requirements, recruitment strategies, and tactics</li>\n<li>Networking through technical journals, publications, social media and the internet</li>\n<li>Client mapping in order to network and build on an existing database</li>\n<li>Continuously source applicants for potential openings; maintain a pipeline of qualified individuals</li>\n<li>Conduct screening interviews to identify qualified candidates</li>\n<li>Provide meaningful feedback and recommendations on candidates to the Client Facing Recruiters</li>\n<li>Identify candidates for key positions, and develop the relationship required to effectively recruit for current or future positions</li>\n<li>The Sourcing Recruiter will work in conjunction with Talent Acquisition Business Partner’s to post open positions and publicize the role within social media forums, job boards, universities or other channels</li>\n<li>Work with Talent Acquisition Business Partner’s to engage with Hiring Managers to gain a better understanding of the recruiting needs</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Undergraduate degree with experience as a Sourcing Recruiter on a Talent Acquisition team or comparable experience</li>\n<li>Demonstrates knowledge of roles within ICON and the ability to communicate these effectively with external candidates</li>\n<li>Previous experience recruiting passive candidates in highly competitive markets in the United States and Canada required</li>\n<li>Proven ability to identify suitable candidates and match them to open positions in the USA and Canada</li>\n<li>Has knowledge of recruitment databases, applicant tracking systems and external job websites</li>\n<li>Demonstrates the ability to screen external candidates effectively and provide interview notes</li>\n<li>Experience in the clinical research, pharmaceutical or healthcare industry in a senior recruitment capacity is preferred</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Talent-Sourcing-Recruiter_JR160675-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Talent-Sourcing-Recruiter_JR160675-1","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"contract","x-salary-range":null,"x-skills-required":["recruitment databases","applicant tracking systems","external job websites","sourcing and hunting for talent"],"x-skills-preferred":["experience in the clinical research, pharmaceutical or healthcare industry"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-26T16:01:43.540Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"CONTRACTOR","occupationalCategory":"Human Resources","industry":"Healthcare","skills":"recruitment databases, applicant tracking systems, external job websites, sourcing and hunting for talent, experience in the clinical research, pharmaceutical or healthcare industry"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e0f6767c-42c"},"title":"Integrated Study Timeline Manager","description":"<p>ICON is seeking an Integrated Study Timeline Manager to join their team. 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management, Risk identification and management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_4d7a54e6-782"},"title":"Senior CRA / CRA II","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Clinical Research Associate or Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Research-Associate_JR162178","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Research-Associate_JR162178","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial processes","ICH-GCP guidelines","organisational skills","communication skills"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work 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You will be responsible for increasing market awareness, sales and profitability by increasing the number of new Requests for Proposals (RFPs).</p>\n<p><strong>Primary Responsibilities</strong></p>\n<ul>\n<li>Increase market awareness, sales and profitability by increasing the number of new Requests for Proposals (RFPs)</li>\n<li>Work closely with Account Executives and engagement partners to create a plan to enhance new account penetration, meetings, and RFPs</li>\n<li>Call new and existing accounts and schedule meetings for the business development team</li>\n<li>Regularly follow-up with prospective clients to build meaningful relationships</li>\n<li>Maintain and manage CRM with all activity</li>\n<li>Generate reports to highlight RFPs, meetings, and new account penetration</li>\n<li>Research accounts and identify new opportunities for ICON</li>\n<li>Provide updates to the business development team on activity and conversations with clients</li>\n<li>Generate client interest for potential webinars, industry meetings and conferences</li>\n<li>Review metrics on a regular basis to assess productivity</li>\n<li>Attend internal meetings to discuss new opportunities and the sales pipeline</li>\n<li>Support the preparation for client meetings</li>\n<li>Develop a sales methodology and strategy for increasing new account penetration</li>\n<li>Learn messaging around ICON’s differentiators</li>\n<li>Lead calls and participate in client meetings</li>\n<li>Execute against a specific account plan; routinely achieving quarterly objectives</li>\n</ul>\n<p><strong>To be Successful in the Role, you will have:</strong></p>\n<ul>\n<li>Undergraduate degree or its international equivalent from an accredited institution or equivalent experience</li>\n<li>Pre / inside sales experience or related experience that requires communicating with potential clients</li>\n<li>Strong verbal and written communication skills</li>\n<li>Familiarity with maintaining and managing a customer relationship database</li>\n<li>Preferably 1-2 years of CRO experience</li>\n</ul>\n<p><strong>What ICON can offer you:</strong></p>\n<p>Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary and OTE, ICON offers a range of additional benefits.</p>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Account-Development-Manager_JR161433","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Account-Development-Manager_JR161433","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["sales","communication","CRM management","account development"],"x-skills-preferred":["CRO experience","healthcare industry knowledge"],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-12T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Sales","industry":"Healthcare","skills":"sales, communication, CRM management, account development, CRO experience, healthcare industry knowledge"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b10d13c2-3f9"},"title":"Senior Manager, Quality Assurance","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Manager, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will manage quality assurance and compliance activities across your area, ensuring your team delivers to the highest standards. 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Key responsibilities include:</p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Willingness to travel as required (approximately 30-50%)</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-CRA_JR156398","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://iconplc.com/careers","logo":"https://logos.yubhub.co/iconplc.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-CRA_JR156398","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical trial monitoring","data integrity","site management"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-26T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blue Bell (ICON"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical trial monitoring, data integrity, site management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b7d68cbd-b81"},"title":"Healthcare Improvement Project Manager","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As the world&#39;s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.</p>\n<p>The Project Manager (HCI Program &amp; 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understand relevant internal/external funding regulations well enough to catch compliance issues early</li>\n<li>Compile, organize, and quality-check data and materials for HCI measurement and reporting, working with the HCI Lead to ensure metrics reflect both system-level change and patient-level outcomes</li>\n<li>Prepare and help synthesize materials for external meetings, internal leadership discussions, HCI Steering Committees and other governance forums; capture decisions and action items and drive follow-through</li>\n<li>Help maintain the HCI technology/ecosystem tools (e.g., trackers, dashboards, collaboration platforms) used to manage the portfolio</li>\n<li>Lead landscape analyses of new disease state, new HCI area of focus or new approach</li>\n<li>Identify opportunities to standardize or streamline recurring operational processes across the HCI portfolio and bring forward improvement ideas rather than waiting to be told what to fix</li>\n<li>Additional operational tasks as warranted by portfolio demands and HCI Lead needs</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree.</li>\n<li>5+ years of program/project management experience, ideally supporting complex, multi-stakeholder initiatives.</li>\n<li>Direct experience or meaningful exposure to healthcare, healthcare systems, or health-related programs (e.g., prior work in/with health systems, payers, provider organizations, public health, medical societies, or pharma/biotech).</li>\n<li>Demonstrated ability to manage budgets, timelines, and multiple workstreams simultaneously with high attention to detail and follow-through.</li>\n<li>Exposure to quality improvement, performance improvement, or implementation-improvement science methodology (even if not the primary role) , e.g., familiarity with IHI models, PDSA cycles, or similar frameworks</li>\n<li>Ability to influence with diplomacy</li>\n<li>High level of experience with Claude and/or Co-pilot</li>\n<li>Experience with public-private partnerships</li>\n<li>Experience in managing relationship and work plans with external partners</li>\n</ul>\n<p><strong>Rewards &amp; 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