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

Overview

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

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model centers on the patient and the customer, with a focus on simplifying and streamlining work. This is a remote role on a sponsor-dedicated team that drives biomarker and bioanalytical strategy across global clinical trials.

Discover what our 29,000 employees across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
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• Lead Biomarker Study Operations
  • Oversee biomarker and bioanalytical 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 development plans
  • Plan and manage collection, tracking, and analysis of biological specimens
  • Advise study teams on sample management and logistics best practices
• Drive Clinical Project Delivery
  • Lead cross-functional teams through the full clinical trial lifecycle (start-up to closeout)
  • Ensure studies stay on track for timelines, budget, scope, and quality
  • Act as main liaison between the sponsor and study partners
  • Monitor and manage project financials; ensure fiscal responsibility
  • Identify and resolve operational issues and risks proactively
• Ensure Operational Excellence
  • Maintain high-quality documentation, including 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
• Independent work style and openness to new technologies
• Willingness to travel up to 25% as needed

• Meaningful Work: Your contributions support biomarker research shaping clinical development and precision medicine.
• Global Impact: Work on high-profile studies across regions, impacting patients worldwide.
• Dedicated Team: Collaborative, sponsor-dedicated environment where your expertise is valued.
• Flexibility: Fully remote role with structured team support.
• Professional Growth: Career development, mentorship, and leadership opportunities.
• Stability and Vision: Part of a leading global organization with a track record of partnerships in clinical research.

If you’re passionate about clinical research and biomarker science, we’d love to hear from you. Apply now to be part of a team shaping the future of clinical development.

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. We also encourage joining our Talent Network to stay connected to additional career opportunities.

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, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status. If you require reasonable accommodation to complete any part of the application process, please contact us at:

Roles within Clinical Project Management at the M23 level plan, direct, create, and communicate clinical study timelines. They gather input from cross-functional teams to ensure deliverables are produced on schedule, maintain consistency across trials, and oversee operational aspects in accordance with SOPs, GCP, and country regulations. Responsibilities include site and vendor selection, budget preparation, and monitoring progress. They may develop trial recruitment strategies in alignment with clinical development strategy.

For more information about Syneos Health, visit