🧫 Job Title: Clinical Project Manager II – Biomarker Study Management
Type: Sponsor-Dedicated | Remote
Location: USA (Remote)
Job ID: 25102536
Updated: November 10, 2025
🌍 About Syneos Health
Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization that accelerates customer success through clinical, medical affairs, and commercial insights.
With over 29,000 employees across 110 countries, Syneos Health brings together patients, science, and strategy to transform how therapies are developed and delivered.
Our mission:
To simplify and streamline clinical research by putting the customer and patient at the center of everything we do.
Our culture:
Passionate problem-solvers driving innovation
Committed to a Total Self Culture — where every employee can authentically be themselves
Diverse, inclusive, and globally connected
Focused on professional growth, collaboration, and operational excellence
🎯 Position Overview
We are hiring a Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated) to lead biomarker and bioanalytical operations within global clinical trials.
This fully remote role offers the opportunity to drive success in biomarker-based research by leading cross-functional teams, managing vendors, and ensuring clinical and bioanalytical excellence across studies (Phases I–IV).
⚙️ Key Responsibilities
1. Lead Biomarker Study Operations
Oversee biomarker and bioanalytical activities across sponsor and collaborative programs.
Serve as the primary operational contact for all biomarker-related processes.
Integrate biomarker strategies into clinical development plans.
Plan, track, and manage biological sample collection and analysis.
Advise study teams on sample management best practices and logistics.
2. Drive Clinical Project Delivery
Lead cross-functional teams throughout the entire clinical trial lifecycle (start-up to closeout).
Maintain timeline, budget, scope, and quality adherence.
Act as liaison between sponsor and study partners.
Monitor project financials and ensure fiscal accountability.
Identify and resolve operational risks proactively.
3. Ensure Operational Excellence
Maintain audit-ready documentation and ensure Trial Master File (TMF) completeness.
Keep study systems and databases updated and compliant.
Prepare and present project reports and updates for stakeholders.
Lead internal and external meetings to ensure alignment.
Support regulatory compliance and inspection readiness.
👩🔬 Required Qualifications & Skills
Education
Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related discipline.
Equivalent combinations of education and experience may be considered.
Experience
Significant experience managing biomarker studies and external vendors.
Deep understanding of biomarker and bioanalytical strategies in clinical trials.
Proven ability to manage complex sample workflows and logistics.
Prior experience in a CRO or sponsor environment preferred.
Technical & Professional Skills
Knowledge of GCP, ICH guidelines, and global regulatory standards.
Excellent project management, organizational, and communication skills.
Strong capability in cross-functional coordination and problem-solving.
Proficient in using digital tools and modern project management platforms.
Ability to work independently and remotely.
Willingness to travel up to 25% as required.
🌟 Why Join Syneos Health
Meaningful Work
Directly contribute to advancing biomarker science and shaping the future of precision medicine.
Global Impact
Work on high-profile, multi-regional studies that improve patients’ lives worldwide.
Dedicated Team
Collaborate within a sponsor-dedicated environment where expertise is valued and voices are heard.
Flexibility
Enjoy the benefits of a fully remote role supported by a connected and responsive team.
Professional Growth
Access continuous learning, mentorship, and leadership opportunities.
Stability & Vision
Be part of a globally recognized leader known for operational excellence and innovation in clinical research.
💰 Compensation & Benefits
Salary Range: $95,000 – $175,700 USD annually
(Actual salary based on qualifications, experience, and skills)
Bonus Eligibility: Discretionary performance-based annual bonus
Benefits Include:
Health (Medical, Dental, Vision)
401(k) company match
Employee Stock Purchase Plan (ESPP)
Paid Time Off (PTO) and Sick Leave
Flexible work-life balance options
Eligibility for car allowance or company car (role-dependent)
🧩 Summary of Role Impact (M23 Level)
Core Responsibilities
Plan, direct, and communicate clinical study timelines
Ensure operational consistency across multiple trials
Maintain adherence to SOPs, GCP, and country regulations
Oversee vendor and site selection
Manage clinical trial budgets and progress tracking
Implement recruitment and development strategies
Impact
Clinical Project Managers at this level are pivotal in ensuring studies are conducted efficiently, effectively, and compliantly, safeguarding data integrity and advancing global clinical research efforts.
🌐 About Syneos Health’s Global Impact
Partnered in 94% of all FDA-approved novel drugs in the last 5 years
Involved in 95% of EMA-authorized products
Supported 200+ studies across 73,000 sites and 675,000+ patients globally
Visit 🔗 www.syneoshealth.com to learn more.
⚖️ Equal Opportunity Statement
Syneos Health is an equal opportunity employer, committed to diversity, inclusion, and authenticity in the workplace.
We welcome applicants from all backgrounds — even if your experience doesn’t align perfectly, transferable skills are valued.
If you require reasonable accommodation for any part of the application process, Syneos Health will provide support consistent with the Americans with Disabilities Act (ADA).
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