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This role also provides technical leadership across troubleshooting, method transfer, and cross-functional collaboration to support scalable laboratory operations.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Plan assay and method development activities and draft clear, robust laboratory methods</li>\n<li>Execute method development experiments and support validation and analytical testing activities as needed</li>\n<li>Troubleshoot assays and apply root cause analysis to optimize performance and resolve technical issues</li>\n<li>Transfer methods into validation processes and collaborate across functions to ensure methods are sustainable and scalable</li>\n<li>Lead low to moderately complex technical projects and guide assigned team members to achieve project deliverables</li>\n<li>Mentor and train junior staff while contributing technical expertise to scientific reports, presentations, and documentation</li>\n<li>Support laboratory equipment maintenance, operational standards, and evaluation of new instrumentation</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline is required</li>\n<li>4 years of related experience in method or assay development or specific methodology area</li>\n<li>2 years&#39; experience working with flow cytometry</li>\n<li>Familiarity and working knowledge of immunology</li>\n<li>Sound knowledge of assay/method development and scientific principles, theories, concepts, and state of the art instrumentation</li>\n<li>Experience with method validation, assay troubleshooting, and transfer of methods into laboratory operations</li>\n</ul>\n<p><strong>Preferred Skills:</strong></p>\n<ul>\n<li>Strong troubleshooting and advanced problem-solving skills, including application of root cause analysis</li>\n<li>Effective communication and presentation skills with the ability to work successfully across functions, and comfortable training others</li>\n<li>Strong organizational skills and close attention to detail in a regulated laboratory environment</li>\n<li>Ability to manage multiple tasks independently and bring projects to completion within timeline expectations</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients</li>\n</ul>\n<p><strong>What We Offer:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Senior-Scientist---Translational-Science-Lab--Flow-_R1552924","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Senior-Scientist---Translational-Science-Lab--Flow-_R1552924","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$64,200.00 - $133,600.00","x-skills-required":["flow cytometry","immunology","assay development","method validation","troubleshooting"],"x-skills-preferred":["problem-solving","communication","presentation","organizational","time management"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T01:16:31.719Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Valencia, CA"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"flow cytometry, immunology, assay development, method validation, troubleshooting, problem-solving, communication, presentation, organizational, time management","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":64200,"maxValue":133600,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9b6b65ab-14e"},"title":"Director, Test Code Product & Lifecycle","description":"<p>We are seeking a Director, Test Code Product &amp; Lifecycle to join IQVIA Laboratories. 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Lead advanced database design, analysis, administration and performance optimization to support complex processing needs and future business requirements.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Provide technical leadership and management direction to database administration team members</li>\n<li>Manage resource allocations within a matrix-managed environment</li>\n<li>Lead, plan and oversee state-of-the-art database designs to solve complex database processing problems</li>\n<li>Perform complex database analysis and database design tasks using advanced techniques on the forefront of technology</li>\n<li>Ensure databases meet required operational standards and performance levels, including reliability, response time and query execution time</li>\n<li>Prepare cost analyses and justification for difficult database systems</li>\n<li>Serve as a senior consultant to staff by providing strategic technical advice and consultation on database analysis and design reviews</li>\n<li>Participate in the administration, monitoring, tuning and support of databases in the production environment</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree Computer Science, a related field, or equivalent experience</li>\n<li>Twelve (12) years of information technology experience</li>\n<li>Eight (8) years experience in the database administration area</li>\n<li>Experience in clinical or regulated laboratory environments is helpful</li>\n<li>Experience applying database design approaches that consider existing and future needs, capacity, limitations, operating time and desired results</li>\n<li>Experience evaluating database implementation approaches, backup strategies and recovery strategies</li>\n<li>Knowledge of database administration activities including denormalization, data archival schemes, sizing, data definition language and database objects</li>\n<li>Knowledge of referential integrity, security enforcement and application optimization</li>\n</ul>\n<p><strong>Benefits:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. 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You will also manage several Technical and Husbandry Specialists, while maintaining the highest standards of animal welfare, staff performance, and procedural compliance.</p>\n<p><strong>Main Tasks</strong></p>\n<ul>\n<li>Operational:</li>\n</ul>\n<p>+ Provide operational and people management for a small rodent animal unit   + Ensure compliance with the Animals (Scientific Procedures) Act 1986 (ASPA) and all Home Office, institutional, and ethical requirements   + Act as a holder of a Home Office Personal Licence (PIL) and perform licensed procedures as required   + Oversee animal welfare, husbandry standards, health monitoring, and environmental conditions within the facility   + Support staff training, performance management, and rota planning   + Maintain accurate records relating to animal use, staffing, training, and compliance   + Liaise with scientists, veterinarians, the NACWO, and other Named Persons to support study delivery   + Contribute to continuous improvement of facility processes, SOPs, and regulatory readiness   + Support internal and external audits and inspections   + Keep up to date on latest initiatives concerning animal welfare   + Liaise with external sites, facilities to aid continuous improvement in animal welfare</p>\n<ul>\n<li>People Leader:</li>\n</ul>\n<p>+ Effectively manage direct reports on a day-to-day basis   + Establish strong working relationships across the management community   + Identify areas for improvement and development, and facilitate opportunities for self and direct reports   + Be a positive influence across the group, able to coach, guide, and mentor more junior staff and peers as needed</p>\n<p><strong>Qualifications &amp; Experience</strong></p>\n<ul>\n<li>Degree, HND, or equivalent qualification in a biological or life sciences discipline, or significant equivalent experience in laboratory animal science</li>\n<li>Demonstrable lab-based industry-led experience in the Contract Research Organisation or biotech discovery environment</li>\n<li>Proven leadership or supervisory experience, overseeing smaller teams on a day-to-day basis</li>\n<li>Practical knowledge of standard conditions in animal facilities, including husbandry, biosecurity, environmental controls, and welfare assessment</li>\n<li>Strong communication skills, able to foster working relationships with peers and reports alike in a professional manner</li>\n<li>Home Office Personal Licence covering rodents</li>\n<li>Eligibility and willingness to be appointed as a NACWO under the Animals (Scientific Procedures) Act 1986 (ASPA), subject to Home Office approval</li>\n</ul>\n<p><strong>What We Offer You</strong></p>\n<ul>\n<li>Competitive benefits package starting from day one of employment, covering Financial &amp; Retirement, Health &amp; Wellness, Work-Life Balance, and Additional Perks</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Portishead-United-Kingdom/Associate-Group-Leader---In-Vivo-Unit-Manager_R1567765","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Portishead-United-Kingdom/Associate-Group-Leader---In-Vivo-Unit-Manager_R1567765","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["laboratory animal science","leadership","communication","Home Office Personal Licence","animal welfare"],"x-skills-preferred":["MSc/PhD within relevant discipline","ex vivo biomarker analysis techniques","assay development and validation","project leadership","client communication"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T20:40:35.883Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Portishead"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"laboratory animal science, leadership, communication, Home Office Personal Licence, animal welfare, MSc/PhD within relevant discipline, ex vivo biomarker analysis techniques, assay development and validation, project leadership, client communication"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c7087af1-337"},"title":"Associate BioServices Study Lead - Hybrid","description":"<p>We are seeking an Associate BioServices Study Lead - Hybrid to join IQVIA Laboratories. As an Associate BioServices Study Lead, you will provide scientific oversight throughout the lifecycle of bioanalytical projects while delivering exceptional service to internal and external customers.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Provide scientific oversight for method development, method validation, and sample analysis projects</li>\n<li>Serve as Principal Investigator for GLP studies</li>\n<li>Prepare validation and sample analysis plans, approve experimental designs, and review data for regulatory compliance and scientific quality</li>\n<li>Review validation and bioanalytical reports for completeness and address findings from Quality Control and Quality Assurance reviews</li>\n<li>Monitor assigned projects, communicate status updates, and escalate schedule risks to management</li>\n<li>Investigate failed runs, coordinate method troubleshooting, assemble technical resources, and document investigation findings</li>\n<li>Maintain communication with customers, resolve sample discrepancies, coordinate customer visits, and support quote preparation</li>\n<li>Ensure projects are archived in accordance with IQVIA SOPs and comply with applicable Good Clinical Practice and Good Laboratory Practice standards</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s Degree in a scientific field</li>\n<li>3 years of related experience in a GLP laboratory environment</li>\n<li>Understanding of liquid chromatography combined with mass spectrometry, or in vitro and immunoassay techniques</li>\n<li>Experience with sample extraction, routine laboratory procedures, assay method development, and assay validation</li>\n</ul>\n<p>The Knowledge, Skills and Abilities Needed for This Role:</p>\n<ul>\n<li>Ability to achieve results through effective collaboration with colleagues and cross-functional partners</li>\n<li>Excellent attention to detail, scientific judgment, and written and verbal communication skills</li>\n<li>Ability to interact effectively with internal and external clients while working to defined objectives and timelines</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients</li>\n</ul>\n<p>What We Offer You:</p>\n<ul>\n<li>Competitive salary: $64,200.00 - $133,600.00 per year</li>\n<li>Comprehensive benefits program to support physical, mental and emotional, financial and social well-being</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Associate-BioServices-Study-Lead---Hybrid_R1564880","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Associate-BioServices-Study-Lead---Hybrid_R1564880","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":null,"x-salary-range":"$64,200.00 - $133,600.00","x-skills-required":["liquid chromatography","mass spectrometry","in vitro techniques","immunoassay techniques","sample extraction","assay method development","assay validation"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T09:59:33.253Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis, IN"}},"occupationalCategory":"Healthcare","industry":"Healthcare","skills":"liquid chromatography, mass spectrometry, in vitro techniques, immunoassay techniques, sample extraction, assay method development, assay validation","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":64200,"maxValue":133600,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_eea788a8-c17"},"title":"Clinical Trial Material Manager (2nd Shift)","description":"<p>We are seeking a Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta, GA.</p>\n<p>The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume production environment. This role ensures on-time delivery, quality compliance, staff performance, and continuous improvement while partnering across Project Services, Warehouse, Logistics, Quality, and IT.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Lead, coach, and develop a team of direct reports in a dynamic production environment</li>\n<li>Manage daily and long-range production schedules to meet customer demand and service-level production targets</li>\n<li>Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery</li>\n<li>Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays</li>\n<li>Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting</li>\n<li>Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations</li>\n<li>Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor’s degree, 10 years of experience in lieu of degree</li>\n<li>Minimum 5 years of people management experience, managing 20 employees in a manufacturing environment</li>\n<li>Minimum 5 years of experience managing manual assembly or production lines</li>\n<li>Minimum 2 years of experience leading process improvement projects</li>\n<li>Working knowledge of Microsoft Excel, Outlook, and PowerPoint</li>\n<li>Working knowledge of ICH, GMP, and OSHA regulations</li>\n<li>Six Sigma Yellow or Green Belt experience required; certification preferred</li>\n</ul>\n<p><strong>Knowledge, Skills and Abilities</strong></p>\n<ul>\n<li>Strong leadership, coaching, and staff development skills in a high-volume production environment</li>\n<li>Ability to prioritize urgent and business-critical work while maintaining quality and compliance expectations</li>\n<li>Effective cross-functional communication skills with the ability to escalate risks, constraints, and operational performance updates</li>\n<li>Strong problem-solving skills with the ability to conduct investigations and drive root cause analysis</li>\n<li>Ability to support overtime, weekends, and holidays based on critical business needs and accelerated trial timelines</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<ul>\n<li>Competitive salary: $77,700.00 - $161,800.00 per year</li>\n<li>Comprehensive benefits program, including physical, mental and emotional, financial and social well-being resources</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material-Manager--2nd-Shift-_R1552456","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material-Manager--2nd-Shift-_R1552456","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$77,700.00 - $161,800.00","x-skills-required":["Microsoft Excel","Outlook","PowerPoint","LIMS","ICH","GMP","OSHA","Six Sigma"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-28T04:19:19.190Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Marietta, GA"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"Microsoft Excel, Outlook, PowerPoint, LIMS, ICH, GMP, OSHA, Six Sigma","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":77700,"maxValue":161800,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8ab3b4a6-79b"},"title":"Product Support Technical Advisor II","description":"<p>We are seeking a Product Support Technical Advisor II to join IQVIA Laboratories at Marietta, GA (hybrid).</p>\n<p>Provide senior Tier-3 product support for enterprise laboratory applications and integrated systems supporting U.S.-based lab operations. This role drives rapid resolution of high-impact production incidents, delivers onsite technical troubleshooting, and helps maintain continuity across critical workflows such as kit production, sample processing, and study execution.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Provide advanced Tier 2 and Tier 3 support for LTMS and associated integrated laboratory systems.</li>\n<li>Investigate and resolve complex application, workflow, data, and integration-related issues.</li>\n<li>Serve as the escalation point for support teams handling critical production incidents.</li>\n<li>Support business-critical laboratory operations while minimizing disruption to study execution and client deliverables.</li>\n<li>Collaborate closely with Product, Development, Infrastructure, Cloud, Quality, and Operations teams to drive issue resolution.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in Computer Science, Information Systems, Healthcare Technology, Life Sciences, or related discipline, or equivalent combination of education and experience.</li>\n<li>5+ years of experience supporting enterprise business applications in a production environment.</li>\n<li>Experience investigating and resolving complex application issues.</li>\n<li>Experience working with SQL for data analysis and troubleshooting.</li>\n<li>Experience supporting integrated enterprise applications and business workflows.</li>\n<li>Experience with ServiceNow or comparable IT Service Management platforms.</li>\n<li>Experience supporting production environments with defined SLAs and support processes.</li>\n<li>Create and maintain support documentation, runbooks, knowledge articles, and troubleshooting guides.</li>\n<li>Contribute to onboarding and training materials for support personnel.</li>\n<li>Participate in automation, monitoring, AI-assisted support, and operational improvement initiatives.</li>\n<li>Manage incident queues utilizing ServiceNow and supporting tools.</li>\n<li>Ensure adherence to service level agreements (SLAs) and support metrics.</li>\n<li>Participate in ticket triage, prioritization, escalation management, and queue governance activities.</li>\n<li>Perform detailed troubleshooting and root cause analysis of production issues.</li>\n<li>Analyze application logs, SQL data, integrations, workflows, and business transactions to determine root cause.</li>\n<li>Drive corrective and preventive actions for recurring issues.</li>\n<li>Participate in Problem Management and post-incident reviews.</li>\n<li>Identify opportunities to improve system stability, monitoring, and support processes.</li>\n</ul>\n<p><strong>Preferred Qualifications</strong></p>\n<ul>\n<li>Experience supporting clinical trial, healthcare, pharmaceutical, laboratory, or life sciences applications.</li>\n<li>Experience supporting Laboratory Information Management Systems (LIMS), Laboratory Trial Management Systems (LTMS), or other regulated operational platforms.</li>\n<li>Familiarity with cloud-based application architectures and Azure-hosted environments.</li>\n<li>Experience supporting data integrations, APIs, and enterprise workflow platforms.</li>\n<li>Understanding of clinical trial operations and laboratory business processes.</li>\n<li>Experience with ITIL processes and operational service management.</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<p>We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $57,000.00 - $142,700.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Product-Support-Technical-Advisor-II_R1550660","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Product-Support-Technical-Advisor-II_R1550660","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$57,000.00 - $142,700.00","x-skills-required":["SQL","ServiceNow","IT Service Management","Laboratory Information Management Systems","Laboratory Trial Management Systems","cloud-based application architectures","Azure-hosted environments","data integrations","APIs","enterprise workflow platforms"],"x-skills-preferred":["clinical trial operations","laboratory business processes","ITIL processes","operational service management"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Marietta, GA"}},"employmentType":"FULL_TIME","occupationalCategory":"IT","industry":"Healthcare","skills":"SQL, ServiceNow, IT Service Management, Laboratory Information Management Systems, Laboratory Trial Management Systems, cloud-based application architectures, Azure-hosted environments, data integrations, APIs, enterprise workflow platforms, clinical trial operations, laboratory business processes, ITIL processes, operational service management","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":57000,"maxValue":142700,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_32b196af-281"},"title":"Associate Manager","description":"<p>We are seeking an Associate Manager to join our team at IQVIA Laboratories, a comprehensive global central laboratory services provider supporting clinical trials worldwide.</p>\n<p>As an Associate Manager, you will be responsible for supervising a team of lab staff and ensuring effective operational delivery. Your duties will include:</p>\n<ul>\n<li>Setting day-to-day operational activities for the team with a focus on daily delivery</li>\n<li>Hiring, training, and performance management of staff under the mentorship of management</li>\n<li>Supervising daily activities of assigned laboratory work groups through delegation, technical skills training, and work supervision</li>\n<li>Ensuring activity in the team meets safety guidelines and driving individual accountability for safety</li>\n<li>Reviewing laboratory metrics to identify initiatives and establishing additional metrics such as cost savings</li>\n<li>Ensuring policies, practices, and procedures are understood and followed by direct reports, customers, and stakeholders</li>\n<li>Assisting in the establishment and revision of laboratory policies and procedures</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a human biology-based science</li>\n<li>4 years of relevant experience in a clinical laboratory or clinical trials environment (biochemistry-based)</li>\n<li>Experience in technical leadership and cross-functional collaboration</li>\n<li>Proficiency with LIMS and other laboratory data systems</li>\n<li>Familiarity with CAPA processes and quality systems</li>\n<li>Ability to analyze and interpret complex data</li>\n<li>Ability to effectively coordinate and execute multiple tasks or projects simultaneously</li>\n<li>Ability to effectively write scientific and technical documents</li>\n<li>Understanding of LEAN 6 Sigma principles</li>\n</ul>\n<p>Benefits of joining IQVIA:</p>\n<ul>\n<li>Global exposure</li>\n<li>Variety of therapeutic areas</li>\n<li>Collaborative and supportive team environment</li>\n<li>Access to cutting-edge and innovative in-house technology</li>\n<li>Excellent career development and progression opportunities</li>\n<li>Work-life balance with a strong focus on positive well-being</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Livingston-West-Lothian-United-Kingdom/Associate-Manager---1-x-Immunology-and-1-x-Biochem_R1539272","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Livingston-West-Lothian-United-Kingdom/Associate-Manager---1-x-Immunology-and-1-x-Biochem_R1539272","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["LIMS","CAPA processes","quality systems","LEAN 6 Sigma principles","data analysis","scientific writing"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-06T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Livingston, West Lothian"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"LIMS, CAPA processes, quality systems, LEAN 6 Sigma principles, data analysis, scientific writing"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1e34a5e6-9bd"},"title":"Purchasing Analyst 1","description":"<p>IQVIA Laboratories is a global leader in drug discovery and development laboratory services. 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Troubleshoot issues to resolution.</li>\n<li>Use system reporting and bespoke analysis in Excel and/or Power BI to drive decision making and prioritization.</li>\n<li>Extract spend data from accounts payable or other databases and create spend reports.</li>\n<li>Undertake RFP/RFQ work for competitively tendered business opportunities.</li>\n<li>Perform competitive analysis on supplier bids.</li>\n<li>Prepare and present regular and ad-hoc purchasing recommendations to purchasing management.</li>\n<li>Undertake Purchasing system UAT support activities as assigned.</li>\n<li>Perform other duties as assigned.</li>\n</ul>\n<p><strong>Essential Functions:</strong></p>\n<ul>\n<li>Extract and analyze spend data from Accounts Payable and other internal databases to develop accurate and actionable spend reports.</li>\n<li>Obtain and consolidate spend files from external vendors to establish baseline spend across key purchasing categories.</li>\n<li>Partner with functional stakeholders to gather requirements, define purchasing process steps, and establish project timelines.</li>\n<li>Benchmark and validate sourcing opportunities through Requests for Information (RFIs), develop and issue competitive Requests for Proposals (RFPs), and support negotiation of optimal commercial terms.</li>\n<li>Prepare and present purchasing recommendations, insights, and sourcing outcomes to purchasing management.</li>\n<li>Under guidance, collect and analyze IQVIA data from issue logs to support vendor performance reporting, and coordinate monthly and quarterly vendor management meetings.</li>\n<li>Ensure purchase orders align with contract terms and contribute to continuous improvement of the procure to pay (P2P) process.</li>\n<li>Perform additional duties and support special projects as assigned.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree required; field of study in Business, Supply Chain, Finance, or related discipline preferred.</li>\n<li>Minimum 3 years of professional experience, including at least 1 year in purchasing, procurement, supply chain management, materials management, or a related function involving RFP processes; or an equivalent combination of education, training, and experience.</li>\n<li>Strong knowledge of purchasing methodologies, principles, processes, and best practices.</li>\n<li>Proficiency with Microsoft Office applications, particularly Excel for data analysis and reporting.</li>\n<li>Solid technical accounting understanding and ability to interpret financial data.</li>\n<li>Strong analytical and numeracy skills, with the ability to extract insights from complex datasets.</li>\n<li>Ability to identify financial or process issues and support the development of mitigating actions.</li>\n<li>Demonstrated ability to prioritize, organize, and manage multiple workstreams to meet deadlines in a fast-paced environment.</li>\n<li>Strong interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, vendors, and cross-functional partners.</li>\n<li>Experience with procurement systems (e.g., PeopleSoft, Coupa) is highly desirable.</li>\n<li>Familiarity with LEAN, automation, or process improvement initiatives is a plus.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bratislava-Slovakia/Purchasing-Analyst-1_R1542317","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bratislava-Slovakia/Purchasing-Analyst-1_R1542317","x-work-arrangement":null,"x-experience-level":"entry","x-job-type":"full-time","x-salary-range":"€18,900.00 - €28,300.00","x-skills-required":["Microsoft Office","Excel","procurement systems","data analysis","reporting","supplier performance management","pricing negotiation"],"x-skills-preferred":["PeopleSoft","Coupa","LEAN","automation","process improvement initiatives"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T23:30:15.085Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bratislava"}},"employmentType":"FULL_TIME","occupationalCategory":"Finance","industry":"Healthcare","skills":"Microsoft Office, Excel, procurement systems, data analysis, reporting, supplier performance management, pricing negotiation, PeopleSoft, Coupa, LEAN, automation, process improvement initiatives","baseSalary":{"@type":"MonetaryAmount","currency":"EUR","value":{"@type":"QuantitativeValue","minValue":18900,"maxValue":28300,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8c70d6c1-e46"},"title":"Clinical Lab Scientist (CLS) – Automated Chemistry","description":"<p>We are seeking a Clinical Lab Scientist (CLS) – Automated Chemistry to join IQVIA Laboratories at Valencia, CA.</p>\n<p>As a Clinical Lab Scientist, you will provide professional and technical expertise to perform automated and manual clinical laboratory testing within the Automated Chemistry area, ensuring accurate and timely results that support clinical research and patient care.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Perform and report automated and manual clinical laboratory testing with minimal supervision</li>\n<li>Verify quality control results and release laboratory results in accordance with licensing and regulatory requirements</li>\n<li>Maintain laboratory inventory, prepare reagents, and ensure equipment and testing materials are available for daily operations</li>\n<li>Troubleshoot laboratory processes and communicate testing irregularities that may impact results</li>\n<li>Support assay validations, assay improvements, and implementation of new testing configurations</li>\n<li>Maintain compliance with CLIA, CAP, GCLP, safety, quality, and company procedures</li>\n<li>Participate in audits, inspections, continuing education, and training activities</li>\n<li>Support special projects and other laboratory responsibilities as assigned</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Valid Clinical Laboratory Science (CLS) license required</li>\n<li>Bachelor&#39;s Degree required</li>\n<li>Up to 5 years of relevant experience in a regulated laboratory</li>\n<li>Working knowledge of Good Clinical Laboratory Practices (GCLP), CLIA requirements, and applicable regulatory standards</li>\n<li>Proficiency with complex laboratory testing procedures, laboratory instrumentation, and quality control processes</li>\n</ul>\n<p><strong>Knowledge, Skills and Abilities:</strong></p>\n<ul>\n<li>Strong technical knowledge of clinical laboratory procedures, troubleshooting techniques, and laboratory safety practices</li>\n<li>Effective organizational, communication, and interpersonal skills with the ability to manage multiple priorities</li>\n<li>Strong attention to detail and ability to establish productive working relationships with coworkers, managers, and clients</li>\n</ul>\n<p><strong>Physical Demands:</strong> Ability to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints).</p>\n<p><strong>What We Offer:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Clinical-Lab-Scientist--CLS----Automated-Chemistry_R1559548","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Clinical-Lab-Scientist--CLS----Automated-Chemistry_R1559548","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":"$46,200.00 - $96,200.00","x-skills-required":["Clinical Laboratory Science","GCLP","CLIA","CAP","laboratory testing procedures","laboratory instrumentation","quality control processes"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T21:42:11.603Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Valencia, CA"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Laboratory Science, GCLP, CLIA, CAP, laboratory testing procedures, laboratory instrumentation, quality control processes","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":46200,"maxValue":96200,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_007955f8-da6"},"title":"Specimen Management Associate 2","description":"<p>We are seeking a Specimen Management Associate 2 to join IQVIA Laboratories in Indianapolis, Indiana.</p>\n<p>The Specimen Management Associate 2 supports the accurate receipt, identification, storage, and shipment of clinical specimens. This role also guides entry-level staff on routine procedures and serves as a point of contact for basic troubleshooting and problem resolution.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Accession, sort, label, store, and prepare clinical specimens for testing or shipment</li>\n<li>Maintain freezers, specimen inventories, supplies, compounds, and control materials as assigned</li>\n<li>Identify errors and potential specimen-management issues, resolving routine problems or escalating them to senior staff</li>\n<li>Guide entry-level employees on department procedures and assist with onboarding new team members</li>\n<li>Respond to after-hours alarms and other job-critical situations as required</li>\n<li>Support laboratory safety, quality, and 6S requirements and initiatives</li>\n<li>Communicate clearly, accurately, and promptly with cross-functional stakeholders</li>\n<li>Perform work in accordance with company procedures and applicable regulatory requirements</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>A high school diploma or equivalent is required</li>\n<li>At certain CAP/CLIA laboratory locations, a bachelor&#39;s degree in chemistry, biology, or medical laboratory technology is required</li>\n<li>Six months of related experience is preferred</li>\n<li>Basic knowledge of internal systems and procedures, with the demonstrated ability to navigate and resolve routine challenges</li>\n<li>Working knowledge of specimen accessioning, shipment, storage, inventory maintenance, and problem-resolution procedures</li>\n<li>Basic computer skills</li>\n</ul>\n<p><strong>Benefits:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p><strong>Salary:</strong> The potential base pay range for this role, when annualized, is $35,900.00 - $74,800.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Specimen-Management-Associate-2--First-Shift-_R1572804","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Specimen-Management-Associate-2--First-Shift-_R1572804","x-work-arrangement":"onsite","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":"$35,900.00 - $74,800.00","x-skills-required":["specimen management","laboratory safety","quality control","communication skills"],"x-skills-preferred":["bachelor's degree in chemistry","biology","medical laboratory technology"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-21T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis, Indiana"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"specimen management, laboratory safety, quality control, communication skills, bachelor's degree in chemistry, biology, medical laboratory technology","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":35900,"maxValue":74800,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_3adb4e7f-dde"},"title":"Senior Scientist, Large Molecule Bioanalytical","description":"<p>We are seeking a Senior Scientist, Large Molecule Bioanalytical to join IQVIA Laboratories in Indiana.</p>\n<p>Organize, curate, and scientifically evaluate large molecule, new modality, and biomarker LC/MS data generated in early drug discovery ADME studies. Ensure that complex datasets are accurate, consistent, traceable, and translated into actionable insights that support compound profiling, lead optimization, and data-driven program decisions.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Manage and curate LC/MS datasets from non-regulatory ADME bioanalysis studies supporting exploratory and pilot toxicology in vivo PK/PD studies</li>\n<li>Ensure the accuracy, completeness, consistency, and traceability of data from raw LC/MS outputs through processed results and internal reports</li>\n<li>Perform scientific quality-control reviews to identify outliers, errors, and analytical or method-related artifacts</li>\n<li>Evaluate ADME parameters across compounds, projects, and assay formats to support structure-activity and structure-property relationships</li>\n<li>Collaborate with DMPK, analytical, informatics, and project teams to interpret data and improve pipelines, automation, visualization tools, and analytical efficiency</li>\n<li>Coordinate internal and external CRO data contributions while maintaining alignment among study designs, metadata, analytical methods, and final outputs</li>\n<li>Prepare clear summaries, tables, figures, dashboards, and integrated discovery data packages to support compound progression and portfolio decisions</li>\n<li>Establish standardized data formats, naming conventions, metadata practices, and reproducible workflows for downstream analysis and knowledge sharing</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor’s or master’s degree in analytical chemistry, pharmacokinetics, pharmaceutical sciences, biochemistry, or a related scientific field</li>\n<li>3–7+ years of experience working with LC/MS data in discovery stage ADME or DMPK settings</li>\n<li>Strong understanding of LC/MS workflows, quantitative data analysis, and common discovery ADME assays</li>\n<li>Experience evaluating data quality and identifying analytical, method-related, and data-processing artifacts</li>\n<li>Familiarity with high-resolution mass spectrometry bioanalytical data and workflows for large molecules, new drug modalities, or biomarkers</li>\n</ul>\n<p><strong>The Knowledge, Skills and Abilities Needed for This Role</strong></p>\n<ul>\n<li>Strong analytical thinking and the ability to translate complex scientific datasets into clear, actionable insights</li>\n<li>Scientific rigor, attention to detail, and a strong data-integrity mindset when managing complex datasets</li>\n<li>Effective cross-functional collaboration with bioanalytical scientists, DMPK teams, project coordinators, study directors, CROs, informatics teams, and IT partners</li>\n<li>Ability to communicate data assumptions, limitations, trends, inconsistencies, and conclusions clearly to scientific stakeholders</li>\n<li>Strong organizational skills and the ability to establish standardized, reproducible data-management practices</li>\n<li>Knowledge of bioanalytical workflows for modalities such as oligonucleotides, proteins, peptides, antibody-drug conjugates, ionizable lipids in lipid nanoparticles, and amino acids</li>\n</ul>\n<p><strong>What We Offer You</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. 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You will collaborate with clients and cross-functional teams to deliver scientifically rigorous solutions supporting drug development programs.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Serve as Primary Investigator on scientific client studies, conducting laboratory work and communicating progress and results</li>\n<li>Design and execute complex method development experiments for large-molecule therapeutic candidates</li>\n<li>Evaluate and implement new bioanalytical methods, technologies, and instrumentation for client programs</li>\n<li>Prepare technical summary reports, proposals, and protocols, including reports that may support FDA submissions</li>\n<li>Provide meaningful data analysis and interpretation, including statistical analysis of experimental findings</li>\n<li>Manage multiple complex technical projects and guide or mentor junior scientific staff</li>\n<li>Collaborate across functions to deliver client studies and deploy methods across multiple programs</li>\n<li>Maintain laboratory notebooks, equipment standards, and compliance with applicable SOPs, regulatory requirements, and good documentation practices</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or a related field preferred; 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We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Scientist--Lab-Operations_R1572685","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Scientist--Lab-Operations_R1572685","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":"$46,200.00 - $96,200.00","x-skills-required":["Good Laboratory Practices","laboratory instrumentation","Microsoft Office Suite","scientific protocols"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-22T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis, IN"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"Good Laboratory Practices, laboratory instrumentation, Microsoft Office Suite, scientific protocols","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":46200,"maxValue":96200,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_29e48d34-ce7"},"title":"Records Management Associate","description":"<p>We are seeking a Records Management Associate to join our team at IQVIA Laboratories. As a Records Management Associate, you will ensure effective security, storage, and retrieval of all proprietary and client information in accordance with established procedures.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Ensure effective security, storage, and retrieval of all proprietary and client information in accordance with established procedures.</li>\n<li>Use scanning equipment to digitize records.</li>\n<li>Develop and implement strategy for IQVIA Laboratories Sustainability program.</li>\n<li>Provide reference services to internal clients in accordance with Standard Operating Procedures (SOPs) and by maintaining accurate charge-out check-out systems.</li>\n<li>Create files according to established classification system.</li>\n<li>File, maintain and process reports, collections, and validations where applicable.</li>\n<li>Maintain log and enter metadata in database to track status and facilitate accurate retrieval of information.</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Experience in an office environment.</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers and clients, vendors, internal and external clients.</li>\n<li>Strong organization and planning skills.</li>\n<li>Knowledge of word processing, spreadsheets, and database applications.</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Global exposure</li>\n<li>Variety of therapeutic areas</li>\n<li>Collaborative and supportive team environment</li>\n<li>Access to cutting-edge and innovative, in-house technology</li>\n<li>Excellent career development and progression opportunities</li>\n<li>Work-Life Balance, with a strong focus on a positive well-being.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Livingston-West-Lothian-United-Kingdom/Records-Management-Associate_R1574425","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Laboratories","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Livingston-West-Lothian-United-Kingdom/Records-Management-Associate_R1574425","x-work-arrangement":"onsite","x-experience-level":null,"x-job-type":"contract","x-salary-range":null,"x-skills-required":["office administration","organization","planning","word processing","spreadsheets","database applications"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-16T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Livingston, West Lothian"}},"employmentType":"CONTRACTOR","occupationalCategory":"Operations","industry":"Healthcare","skills":"office administration, organization, planning, word processing, spreadsheets, database applications"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d9cce5d2-9e7"},"title":"Associate BioServices Study Lead","description":"<p>We are seeking an Associate BioServices Study Lead to join IQVIA Laboratories in Ithaca, NY, in a hybrid role.</p>\n<p>As an Associate BioServices Study Lead, you will serve as the primary point of contact for external customers while providing scientific oversight throughout the lifecycle of bioanalytical projects. Working under Study Lead Management and in partnership with Project Management, you will ensure exceptional customer service and adherence to IQVIA scientific, quality, and regulatory standards.</p>\n<p>Key responsibilities:</p>\n<ul>\n<li>Provide scientific oversight for method development, method validation, and sample analysis activities</li>\n<li>Serve as Principal Investigator for GLP studies and ensure compliance with applicable Good Clinical Practice and Good Laboratory Practice requirements</li>\n<li>Collaborate with Technical Writing, Quality Control, Quality Assurance, and Project Management to complete projects according to agreed schedules</li>\n<li>Review validation plans, sample analysis plans, experimental designs, analytical data, data tables, and bioanalytical reports for completeness, scientific quality, and regulatory compliance</li>\n<li>Maintain daily communication with customers, provide updates on active projects, resolve sample discrepancies, and coordinate and conduct customer visits</li>\n<li>Monitor project progress, provide status updates to management, escalate schedule risks, and submit accurate weekly assessments of resource requirements</li>\n<li>Investigate failed runs, address Quality Control and Quality Assurance findings, coordinate method troubleshooting, engage appropriate technical resources, and document investigation outcomes</li>\n<li>Partner with Business Development to prepare customer quotes, prepare data for external presentations, and ensure projects are archived according to IQVIA standard operating procedures</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s Degree in a scientific field</li>\n<li>3 years of related experience in a GLP laboratory environment</li>\n<li>Understanding of liquid chromatography combined with mass spectrometry, or in vitro and immunoassay techniques</li>\n<li>Experience with sample extraction and routine laboratory procedures</li>\n<li>Understanding of assay method development and validation</li>\n</ul>\n<p>Nice to have:</p>\n<ul>\n<li>Ability to achieve results through collaborative efforts with scientific, quality, project management, business development, and customer teams</li>\n<li>Ability to interact effectively with internal and external clients while working to established objectives and timelines</li>\n<li>Excellent attention to detail and strong written and verbal communication skills</li>\n<li>Ability to follow verbally communicated procedures</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients</li>\n</ul>\n<p>Benefits: We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. 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