🧬 Job Title:
Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote)
Updated:
November 10, 2025
Location:
USA – GA – Remote
Job ID:
25102536
🌐 About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization that partners with clients to accelerate the development and delivery of new therapies.
We combine clinical, medical affairs, and commercial insights to achieve better outcomes and adapt to modern healthcare realities.
With 29,000 employees in over 110 countries, Syneos Health is committed to simplifying clinical development while keeping patients and customers at the heart of everything we do.
💡 Why Work at Syneos Health
Career Development: Continuous learning, mentorship, and growth opportunities.
Inclusive Culture: A Total Self environment where everyone can authentically be themselves.
Global Collaboration: Work with diverse teams and innovative thinkers across the world.
Recognition & Rewards: Peer recognition, leadership support, and total rewards program.
Commitment to Belonging: Diversity of thought and perspective drives success.
WORK HERE MATTERS EVERYWHERE.
🧭 Role Overview
We’re seeking a Clinical Project Manager II with strong biomarker study operations expertise.
This fully remote, sponsor-dedicated role focuses on leading biomarker and bioanalytical strategy for global clinical trials, ensuring the highest operational standards in biological sample management and data delivery.
⚙️ Key Responsibilities
1. Lead Biomarker Study Operations
Manage biomarker and bioanalytical activities across sponsor and collaborative programs.
Serve as the primary operational contact for biomarker-related processes.
Collaborate with clinical study teams (Phases I–IV) to embed biomarker strategies into development plans.
Oversee specimen collection, tracking, shipment, and analysis.
Advise on sample management and logistics best practices.
2. Drive Clinical Project Delivery
Lead cross-functional teams through study start-up, conduct, and closeout.
Manage project scope, budget, timelines, and deliverables.
Act as the main liaison between sponsors, vendors, and internal teams.
Monitor and control financial performance and risk mitigation.
Resolve operational challenges proactively and maintain team alignment.
3. Ensure Operational Excellence
Maintain Trial Master File (TMF) documentation accuracy and completeness.
Keep study systems and databases audit-ready.
Develop and deliver project updates, dashboards, and reports.
Facilitate internal and external meetings with key stakeholders.
Support inspection readiness and compliance with regulatory standards (ICH-GCP).
🧪 Required Skills & Experience
|
Category |
Requirements |
|---|---|
|
Education |
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or equivalent experience. |
|
Experience |
Proven expertise managing biomarker studies and external vendors. |
|
Technical Knowledge |
Strong understanding of biomarker and bioanalytical operations in clinical research. |
|
Project Management |
Skilled in planning, budgeting, risk management, and stakeholder communication. |
|
Regulatory Knowledge |
Familiarity with ICH-GCP, SOPs, and international clinical trial regulations. |
|
Work Environment |
Experience in CRO or sponsor setting preferred. |
|
Personal Attributes |
Highly organized, tech-savvy, and capable of working independently. |
|
Travel Requirement |
Willing to travel up to 25% as needed. |
🌟 Why Join Syneos Health
Meaningful Impact: Directly influence biomarker research that advances precision medicine.
Global Reach: Work on multi-regional studies that transform patient outcomes.
Collaborative Team: Sponsor-dedicated setting where your voice and expertise matter.
Flexible Work: Enjoy a fully remote structure supported by responsive leadership.
Growth Path: Ongoing mentorship and leadership opportunities.
Stability: Join a trusted global CRO with long-term client partnerships.
💰 Compensation & Benefits
Salary Range:
$95,000 – $175,700 (USD)
(Actual pay depends on skills, experience, and qualifications.)
Benefits Package Includes:
Company car or car allowance (depending on role)
Comprehensive Medical, Dental, and Vision insurance
401(k) with company match
Employee Stock Purchase Plan
Performance-based commissions/bonuses
Flexible PTO and paid sick leave (compliant with local laws)
🧩 Summary of Role Impact
Roles at the M23 level within Clinical Project Management are responsible for:
Planning, directing, and communicating clinical study timelines
Overseeing operational and regulatory aspects of clinical trials
Ensuring adherence to SOP, GCP, and country regulations
Leading site/vendor selection and budget preparation
Monitoring project progress and ensuring deliverables stay on schedule
Supporting recruitment strategies and clinical development planning
Impact:
Your leadership directly ensures the efficiency, compliance, and success of global biomarker studies — strengthening clinical research integrity and advancing therapeutic development.
⚖️ Compliance & Equal Opportunity
Syneos Health complies with:
Americans with Disabilities Act (ADA) — providing reasonable accommodations as needed.
Equal Opportunity Employment (EOE) regulations and the EU Equality Directive.
The company reserves the right to modify or expand responsibilities as necessary.
📩 How to Apply
If you’re passionate about clinical research and want to make an impact in biomarker science,
👉 Apply Now or Join our Talent Network to stay connected for future roles.
Learn more: www.syneoshealth.com
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