Job Title:
Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote)
Updated:
November 10, 2025
Location:
USA – NH – Remote
Job ID:
25102536
About Syneos Health®
Syneos Health® is a leading global biopharmaceutical solutions organization focused on accelerating customer success.
We integrate clinical development, medical affairs, and commercial expertise to translate scientific innovation into improved patient outcomes.
Our Clinical Development model prioritizes both the customer and the patient, simplifying and streamlining processes to make collaboration efficient and impactful.
With 29,000 employees across 110 countries, we bring agility, innovation, and passion to advancing life-changing therapies.
Why Work with Us
🌍 Global Impact: We partner with 94% of all novel FDA-approved drugs and 95% of EMA-authorized products in the past five years.
💼 Career Growth: Continuous learning, mentorship, and professional development.
❤️ Total Self Culture: Encouraging authenticity and inclusion across all levels.
🧭 Diversity & Belonging: Valuing diverse thoughts, backgrounds, and perspectives.
🏆 Recognition & Rewards: Competitive benefits and peer recognition programs.
Position Overview
The Clinical Project Manager II – Biomarker Study Management role is fully remote and sponsor-dedicated.
You will lead biomarker study operations, overseeing bioanalytical strategy, sample management, and operational execution across global clinical programs.
This position plays a key leadership role in integrating biomarker strategies into clinical development to drive study success.
Key Responsibilities
1. Lead Biomarker Study Operations
Manage biomarker and bioanalytical activities across sponsor and collaborative programs.
Act as the primary operational contact for all biomarker-related processes.
Collaborate with clinical study teams (Phases I–IV) to integrate biomarker strategies.
Oversee biological sample collection, tracking, and analysis activities.
Provide expert guidance on sample logistics and management best practices.
2. Drive Clinical Project Delivery
Lead cross-functional project teams through the full clinical trial lifecycle — start-up to closeout.
Ensure adherence to timelines, budget, scope, and quality standards.
Serve as the main liaison between the sponsor and study partners/vendors.
Monitor and manage project financials and operational risks proactively.
Identify issues early and implement resolution plans to maintain study progress.
3. Ensure Operational Excellence
Maintain accurate and complete documentation (Trial Master File readiness).
Keep study databases and systems audit-ready and up to date.
Prepare project reports, metrics, and sponsor updates.
Plan and facilitate internal/external stakeholder meetings.
Support inspection readiness and ensure GCP/regulatory compliance throughout the trial.
Skills & Experience Required
|
Qualification Area |
Requirements |
|---|---|
|
Education |
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, or equivalent combination of education and experience. |
|
Experience |
Proven experience in managing biomarker studies and vendor oversight. |
|
Technical Knowledge |
In-depth understanding of biomarker and bioanalytical operations in clinical research. |
|
Project Management |
Strong organizational, communication, and leadership skills. |
|
Regulatory Awareness |
Familiarity with ICH-GCP guidelines and global clinical trial regulations. |
|
Preferred Background |
Previous experience in CRO or sponsor environments. |
|
Work Style |
Independent, proactive, and technology-adaptive professional. |
|
Travel |
Up to 25% travel may be required. |
Why Join Syneos Health
Meaningful Work: Directly contribute to biomarker-driven innovations in precision medicine.
Global Collaboration: Work across international clinical programs with multidisciplinary teams.
Flexibility: Fully remote position with structured team support.
Growth Potential: Access to leadership development and continued training.
Stability & Vision: Join a trusted global CRO with long-term client partnerships.
Compensation & Benefits
Salary Range:
💰 $95,000 – $175,700 (USD)
(Actual compensation will depend on qualifications, skills, and experience.)
Comprehensive Benefits Include:
Company car or car allowance (role-dependent)
Health coverage (Medical, Dental, Vision)
401(k) with company match
Employee Stock Purchase Plan
Performance-based commissions/bonuses
Flexible PTO and sick leave
Compliance with all state/federal paid time regulations
Summary of Role Impact
Core Focus Areas
Planning, directing, and managing clinical study timelines
Overseeing operational aspects and consistency of clinical trials
Adhering to SOPs, GCP, and local regulations
Site and vendor selection
Clinical trial budget planning
Monitoring study progress and deliverables
Supporting clinical development and recruitment strategies
Overall Contribution
This role ensures efficient, compliant, and high-quality biomarker study execution, directly influencing the success and credibility of clinical research outcomes.
Additional Information
The listed responsibilities are not exhaustive and may evolve based on project or sponsor needs.
Syneos Health complies fully with the Americans with Disabilities Act (ADA) and EEO regulations.
Equivalent combinations of education and experience will be considered.
The company reserves the right to modify duties or qualifications as needed.
Apply Now
If you are passionate about biomarker science and want to lead clinical research that changes lives,
👉 Apply today or Join our Talent Network to stay connected with future opportunities.
Learn more: www.syneoshealth.com
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