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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9d3f8c9a-659"},"title":"Site Contracts Lead","description":"<p>Syneos Health is seeking a Site Contracts Lead to manage negotiation of clinical study agreements (CTAs) on a study level and drive CTA document finalization and execution.</p>\n<p>The successful candidate will oversee negotiations of clinical study agreements (CTAs) on a study level and drive CTA document finalization and execution, including contractual language &amp; terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract &amp; budget negotiators.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Oversees negotiations of clinical study agreements (CTA´s) on a study level and drives CTA document finalization and execution, including contractual language &amp; terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract &amp; budget negotiators.</li>\n<li>Provides oversight of contact &amp; budget negotiations status and manages escalation of out-of-parameter queries on budgetary and contractual requests to sponsor decision-makers in all regions of study conduct.</li>\n<li>Acts as first-line subject matter expert for all such CTA elements on assigned studies for internal and sponsor stakeholders alike.</li>\n<li>Plans contract execution strategy for assigned studies,including forecast of site-specific contractual execution timelines with as much accuracy as possible,and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.</li>\n<li>Works closely with internal stakeholders and with Sponsor to prepare site contractual templates, including payment terms, and study-level negotiation parameters and processes within Company standards in order to drive successful negotiation of contracts and budgets.</li>\n<li>Establishes strong working relationships and collaboration with Sponsor to ensure site contractual templates fit into the global strategy set for the program.</li>\n<li>Creates and maintains document status reports, and updates department tools/systems and team members on a regular basis; ensures appropriate documentation is maintained.</li>\n<li>Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.</li>\n<li>Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites.</li>\n<li>May support BU and organization through help desk and other defined pathways to resolve and deescalate issues.</li>\n<li>Performs other work-related duties as assigned.</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>BS degree in life sciences, a health related field, or equivalent combination of education and experience.</li>\n<li>Preferred experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.</li>\n<li>Thorough knowledge of applicable regulations, drug development and clinical project management procedures.</li>\n<li>Good presentation, documentation and interpersonal skills.</li>\n<li>Proficient in MS Office (Word, Excel and PowerPoint), MS Project, outlook and Internet.</li>\n<li>Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment.</li>\n<li>Attention to detail, effective oral/written communication skills along with the ability to work independently to meet deadlines.</li>\n<li>Strong leadership skills; 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The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff, providing recommendations regarding site-specific actions</li>\n<li>Verify process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n<li>Understand project scope, budgets, and timelines, and manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>May act as primary liaison with study site personnel or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</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://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/UKR-Remote/CRAII_25109371","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/UKR-Remote/CRAII_25109371","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"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":"2026-10-19T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"UKR-Remote"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"}]}