Clinical Project Manager II – Biomarker Study Management; Sponsor-Dedicated | Remote

Clinical Project Manager II – Biomarker Study Management (Sponsor‑Dedicated | Remote)

We’re hiring a Clinical Project Manager II with a strong background in biomarker study operations to join our sponsor‑dedicated team. This fully remote role gives you the opportunity to drive the success of global clinical trials by leading biomarker and bioanalytical strategy from start to finish.

• Lead biomarker and bioanalytical activities across sponsor and collaborative programs.
• Serve as the operational point of contact for all biomarker‑related processes.
• Work closely 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 required.
• 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.
• Experience in a 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: directly support biomarker research shaping the future of clinical development.
• Global impact: work on high‑profile studies spanning multiple regions.
• Dedicated team: collaborative sponsor‑dedicated environment where your expertise is trusted.
• Flexibility: fully remote role with structured, responsive team.
• Professional growth: continual learning, mentorship, and leadership opportunities.
• Stability and vision: part of a leading global organization known for operational excellence.

Salary Range: $95,000.00 – $

Apply now and be part of a team shaping the future of clinical development.

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of your application process, please contact us at .