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

0-2 years
$95,000 – $175,700
10 Nov. 12, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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

📅 Updated: November 10, 2025
📍 Location: USA–VT–Remote
🆔 Job ID: 25102536
🏢 Company: Syneos Health®


About Syneos Health®

Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success through clinical, medical, and commercial expertise. With operations in over 110 countries and 29,000 employees, the company partners with clients to improve patient outcomes and drive innovation in healthcare.

Our Clinical Development model puts the customer and patient at the center of everything we do, streamlining processes to deliver therapies faster and more effectively.

Motto:

Work Here Matters Everywhere


Why Syneos Health

  • 🌍 Inclusive Culture: “Total Self” culture encourages authenticity and individuality.

  • 📈 Career Growth: Opportunities for development, progression, and recognition.

  • 🤝 Supportive Management: Engaged leadership, mentorship, and technical training.

  • 🌐 Diversity & Belonging: Collaboration across varied thoughts, backgrounds, and cultures.

  • 💼 Comprehensive Rewards: Competitive pay, total rewards, and flexible work policies.


Position Overview

The Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote) role involves leading global biomarker study operations and ensuring seamless execution of clinical trial projects.

You will manage biological sample collection, analysis, and logistics, ensuring scientific and operational excellence across all phases (I–IV).


Key Responsibilities

1. 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 activities.

  • Collaborate with clinical study teams to integrate biomarker strategies into development plans.

  • Plan, manage, and track biological specimen collection and analysis.

  • Advise teams on best practices for biomarker logistics and data integrity.

2. Drive Clinical Project Delivery

  • Manage cross-functional teams through the clinical trial lifecycle (start-up to closeout).

  • Ensure delivery within defined timelines, budgets, scope, and quality standards.

  • Act as primary liaison between sponsor, vendors, and internal partners.

  • Track and control project financials, addressing variances proactively.

  • Identify and mitigate operational risks and challenges.

3. Ensure Operational Excellence

  • Maintain Trial Master File (TMF) accuracy and audit readiness.

  • Ensure compliance with GCP, ICH, and SOP standards.

  • Prepare and deliver project status reports and sponsor updates.

  • Lead meetings, documentation, and regulatory inspection readiness activities.


Required Skills & Experience

  • Experience: Proven experience managing biomarker studies and external vendors.

  • 🧬 Knowledge: Strong understanding of biomarker and bioanalytical processes in clinical settings.

  • 📦 Expertise: Proficient in coordinating complex sample collection and analytical workflows.

  • 🎓 Education: Bachelor’s in Life Sciences, Medicine, Pharmacy, Nursing, or related field.

  • 💡 Technical: Strong command of clinical systems, reporting tools, and documentation platforms.

  • 🌐 Preferred Background: Prior experience in CRO or sponsor environment.

  • 📜 Regulatory Understanding: Familiar with global GCP, ICH, and compliance requirements.

  • 🧭 Skills: Excellent communication, organization, leadership, and problem-solving.

  • ✈️ Travel: Up to 25% as required.


Why Join Syneos Health

  • 💊 Meaningful Work: Contribute directly to the advancement of precision medicine and biomarker science.

  • 🌎 Global Impact: Manage international studies impacting thousands of patients worldwide.

  • 🤝 Collaborative Team: Work in a supportive sponsor-dedicated environment.

  • 🏠 Flexibility: Fully remote setup with strong organizational support.

  • 🚀 Professional Growth: Access to continuous learning, leadership programs, and mentorship.

  • 🧩 Stability: Join a globally recognized, innovation-driven clinical research leader.


Compensation & Benefits

💰 Salary Range: USD $95,000 – $175,700 (based on qualifications, skills, and experience).
🎁 Benefits Include:

  • Health (Medical, Dental, Vision)

  • 401(k) with Company Match

  • Employee Stock Purchase Plan

  • Paid Time Off (PTO) & Sick Leave (varies by state)

  • Performance-based bonus/commission eligibility

  • Car allowance (where applicable)


About Syneos Health – Global Impact

  • Worked with 94% of all Novel FDA Approved Drugs

  • Supported 95% of EMA Authorized Products

  • Managed 200+ Studies, 73,000 Sites, and 675,000+ Trial Patients

📍 Learn more: www.syneoshealth.com


Additional Information

  • Tasks and responsibilities are not exhaustive; may be modified as needed.

  • Equivalent experience or education may substitute listed qualifications.

  • Syneos Health is an Equal Opportunity Employer, committed to compliance with the Americans with Disabilities Act (ADA) and diversity in the workplace.


Role Summary (M23 Level – Clinical Project Management)

Core Functions:

  • Plan, direct, and communicate clinical study timelines.

  • Oversee operational aspects of clinical trials and ensure consistency across studies.

  • Manage site/vendor selection, budget preparation, and project progress monitoring.

  • Support the clinical development strategy and recruitment planning.

Impact:
Ensures successful, efficient, and compliant execution of global clinical trials — contributing directly to the quality, integrity, and advancement of medical research.


Application

🔗 Apply Now: Join Our Talent Network