🧬 Clinical Project Manager II – Biomarker Study Management
(Sponsor-Dedicated | Remote)
📅 Updated: November 10, 2025
📍 Location: USA–MS–Remote
🆔 Job ID: 25102536
🧩 About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We combine clinical, medical affairs, and commercial insights to transform innovation into outcomes that address today’s healthcare challenges.
Our Clinical Development model places the customer and patient at the center of all we do. We continuously seek new ways to simplify, streamline, and optimize clinical research — making Syneos Health both easier to work with and for.
With 29,000 employees in over 110 countries, we bring together passionate professionals dedicated to changing lives through scientific and operational excellence.
WORK HERE MATTERS EVERYWHERE.
🌎 Why Syneos Health
We’re passionate about the growth and well-being of our people.
What Sets Us Apart
🎓 Career Development & Progression: Continuous learning, technical training, and leadership growth.
🤝 Supportive Management: Engaged leaders who guide, mentor, and recognize performance.
💡 Total Self Culture: Encouraging authenticity — be yourself at work.
🌈 Inclusive Environment: Diverse teams bring creativity, perspective, and belonging.
🏆 Recognition & Rewards: Comprehensive total rewards and peer appreciation programs.
Together, we’re building the company we all want to work for and our customers want to work with.
🎯 Position Overview
The Clinical Project Manager II – Biomarker Study Management plays a key role in sponsor-dedicated biomarker and bioanalytical operations.
You will lead global biomarker study activities across all trial phases, ensuring scientific excellence, operational efficiency, and high-quality outcomes.
This remote position offers the opportunity to collaborate with global cross-functional teams to drive biomarker integration into clinical development.
⚙️ Key Responsibilities
🔬 1. Lead Biomarker Study Operations
Oversee 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 integrate biomarker strategies into overall study design.
Plan, manage, and track biological specimen collection, shipment, and analysis.
Provide guidance on sample management logistics and best practices.
📋 2. Drive Clinical Project Delivery
Lead cross-functional teams through all trial phases — start-up to closeout.
Ensure adherence to timelines, budgets, and quality standards.
Act as the main liaison between sponsors, vendors, and internal teams.
Manage project financials and monitor budgets effectively.
Identify and mitigate operational risks proactively.
⚖️ 3. Ensure Operational Excellence
Maintain audit-ready documentation, ensuring Trial Master File (TMF) accuracy.
Keep study systems, trackers, and databases updated and compliant.
Prepare reports, dashboards, and presentations for internal and sponsor updates.
Lead study meetings (internal/external) and ensure clear communication across teams.
Support inspection readiness and regulatory compliance throughout the project lifecycle.
👩🔬 Skills and Experience
✅ Required
Strong experience managing biomarker studies and coordinating external vendors.
Deep understanding of biomarker and bioanalytical strategies in clinical trial settings.
Proven ability to manage sample collection and analysis workflows.
Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent.
Familiarity with GCP, ICH guidelines, and global regulatory standards.
Excellent communication, leadership, and organizational skills.
Comfortable working independently and adopting new technologies.
Willingness to travel up to 25% as required.
🌟 Preferred
Prior experience in a CRO or Sponsor environment.
💼 Why Join Us
|
Benefit |
Description |
|---|---|
|
💉 Meaningful Work |
Contribute directly to biomarker research that advances precision medicine. |
|
🌍 Global Reach |
Work on large-scale, multi-regional clinical studies. |
|
🤝 Collaborative Culture |
Partner with scientific and operational experts worldwide. |
|
🏠 Remote Flexibility |
Enjoy the balance of a fully remote work model. |
|
🚀 Career Advancement |
Opportunities for leadership growth and specialization. |
|
🏢 Organizational Strength |
Join a trusted leader known for clinical excellence and innovation. |
💰 Compensation & Benefits
Salary Range: $95,000 – $175,700 USD (based on qualifications and experience)
Annual Bonus: Discretionary, performance-based
Benefits Include:
Health: Medical, Dental, Vision
Company Match 401(k)
Employee Stock Purchase Plan (ESPP)
Paid Time Off (PTO) & Sick Leave
Car Allowance or Company Car (as applicable)
Flexible Work Arrangements
Syneos Health complies with all applicable federal, state, and municipal labor laws, including paid sick leave and workplace regulations.
📊 Role Overview (M23 Level – Clinical Project Management)
Core Focus
Plan, direct, and communicate clinical study timelines.
Oversee operational aspects of clinical trials.
Ensure adherence to SOPs, GCP, and country-specific regulations.
Select and manage sites, vendors, and budgets.
Support recruitment strategies and development planning.
Impact & Contribution
Clinical Project Managers at this level ensure timely, compliant, and high-quality trial execution, contributing directly to the success of global clinical programs.
🌐 About Syneos Health’s Global Impact
Partnered in 94% of FDA-approved novel drugs (past 5 years)
Supported 95% of EMA-authorized products
Managed 200+ studies across 73,000 sites and 675,000+ trial patients
🔗 Learn more: www.syneoshealth.com
⚖️ Equal Opportunity Statement
Syneos Health is an Equal Opportunity Employer, committed to diversity, inclusion, and authenticity.
We welcome applicants even if their experience doesn’t perfectly align with all qualifications.
Transferable skills are valued, and reasonable accommodations are available under the Americans with Disabilities Act (ADA).
📝 Additional Information
Responsibilities listed are not exhaustive; additional duties may be assigned.
Equivalent education or experience will be considered.
This job description does not constitute an employment contract.
Syneos Health complies with global labor and equality directives in all hiring practices.
📮 Apply Now
🔹 Apply: Syneos Health Careers
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