Clinical Project Manager II – Biomarker Study Management ; Sponsor Dedicated

Clinical Project Manager II – Biomarker Study Management (Sponsor Dedicated – US Remote; Preference for Hybrid Foster City, CA)

$95,000 - $176,000

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

• Lead biomarker and bioanalytical strategy from start to finish, overseeing activities across sponsor and collaborative programs.
• Serve as the operational point of contact for all biomarker-related processes.
• Collaborate with clinical study teams (Phases 1–4) to integrate biomarker strategies into broader clinical development plans.
• Plan and manage the collection, tracking, and analysis of biological specimens.
• Advise study teams on best practices for sample management and logistics.
• Lead cross‑functional teams through the full clinical trial lifecycle, from start‑up to closeout.
• Ensure studies stay on track with respect to timelines, budget, scope, and quality.
• Act as the main liaison between the sponsor and study partners.
• Monitor and manage project financials, ensuring fiscal responsibility.
• Proactively identify and resolve operational issues and risks.
• Maintain high‑quality documentation, including Trial Master File (TMF) accuracy and completeness.
• Keep study systems and databases current and audit‑ready.
• Prepare project reports and updates for sponsors and internal stakeholders.
• Plan and facilitate internal and external meetings.
• Support inspection readiness and regulatory compliance throughout the project.

• Significant experience managing biomarker studies and external vendors.
• Strong understanding of biomarker and bioanalytical strategies in a clinical trial setting.
• Proven ability to coordinate complex sample collection and analysis workflows.
• Expertise in supporting study teams with sample logistics and operational planning.
• Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience.
• Experience in a clinical research organization (CRO) or sponsor environment preferred.
• Familiarity with GCP, ICH guidelines, and global regulatory standards.
• Strong project management, organizational, and communication skills.
• Comfortable working independently and embracing new technologies.
• Willingness to travel up to 25% as needed.

• Meaningful work that directly supports critical biomarker research shaping clinical development and precision medicine.
• Opportunity to work on high‑profile studies spanning multiple regions, impacting patients worldwide.
• Collaborative, sponsor‑dedicated environment where expertise is trusted and voice matters.
• Investments in career through continued learning, mentorship, and leadership opportunities.
• Stability and vision within a leading global organization known for operational excellence.

$95,000.00 – $

These figures represent the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on qualifications, skills, competencies, and proficiency for the role.

Tasks, duties, and responsibilities listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and responsibilities. Equivalent experience, skills, and/or education may be considered. The Company will determine what constitutes equivalence to the qualifications described. The Company is committed to compliance with the Americans with Disabilities Act, providing reasonable accommodations when appropriate.