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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 Remote 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–OR–Remote
Job ID: 25102536


🧩 About Syneos Health

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We combine clinical, medical affairs, and commercial insights to deliver impactful outcomes that address modern market realities.

Our Clinical Development model centers around the customer and patient, constantly evolving to simplify, streamline, and innovate clinical operations — making Syneos Health easier to work with and for.

With 29,000 employees across 110 countries, we bring together passionate problem solvers, dedicated to changing lives through faster, smarter delivery of therapies.

Work Here Matters Everywhere.


🌍 Why Syneos Health?

At Syneos Health, we believe in the power of our people.
We invest in:

  • 🎓 Career development & progression through training and mentorship

  • 🤝 Supportive, engaged management that values collaboration

  • 💡 Total Self Culture – be your authentic self at work

  • 🌈 Diversity, inclusion, and belonging, uniting people of all backgrounds

  • 🏆 Recognition and rewards through our total rewards program

We’re continuously building a workplace that people want to work for — and clients want to work with.


🎯 Position Summary

We are seeking a Clinical Project Manager II – Biomarker Study Management to join our Sponsor-Dedicated team.

This fully remote role offers the opportunity to lead and manage global biomarker and bioanalytical operations in clinical trials (Phases I–IV).
You’ll play a key role in driving scientific and operational excellence across biomarker studies — from planning and coordination to data delivery.


⚙️ 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 processes.

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

  • Plan, track, and manage the collection, shipment, and analysis of biological specimens.

  • Provide expert guidance on sample management, logistics, and data workflows.


📋 2. Drive Clinical Project Delivery

  • Lead cross-functional teams throughout all study phases — start-up to closeout.

  • Ensure studies meet timelines, budgets, scope, and quality requirements.

  • Serve as liaison between sponsor and external partners/vendors.

  • Monitor and manage project financials with fiscal accountability.

  • Identify and mitigate operational risks proactively.


⚖️ 3. Ensure Operational Excellence

  • Maintain audit-ready documentation (e.g., Trial Master File accuracy and completeness).

  • Keep study systems and databases updated and compliant.

  • Prepare status reports, dashboards, and stakeholder updates.

  • Organize and lead internal and external study meetings.

  • Support regulatory compliance and inspection readiness.


👩‍🔬 Skills & Experience You Bring

Required:

  • Proven experience managing biomarker studies and coordinating external vendors.

  • Deep understanding of biomarker and bioanalytical strategies in clinical trials.

  • Strong expertise in sample collection and analysis workflows.

  • Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent field.

  • Proficiency with GCP, ICH guidelines, and global regulatory standards.

  • Excellent project management, communication, and organizational skills.

  • Comfortable working independently and adapting to new technologies.

  • Willingness to travel up to 25%.

Preferred:

  • Prior experience in a CRO or Sponsor environment.


🌟 Why Join Us

Benefit

Description

💉 Meaningful Work

Contribute to biomarker research that drives precision medicine and clinical innovation.

🌍 Global Impact

Collaborate on multi-regional studies improving patient outcomes worldwide.

🤝 Dedicated Team

Be part of a sponsor-dedicated setup where your voice and expertise are valued.

🏠 Remote Flexibility

Enjoy full remote work with a well-structured support network.

🚀 Career Growth

Access leadership programs, mentoring, and skill development opportunities.

🏢 Stability & Vision

Work for a global leader renowned for operational excellence and innovation.


💰 Compensation & Benefits

  • Base Salary Range: $95,000 – $175,700 USD
    (Varies based on experience, qualifications, and performance)

  • Bonus: Eligible for annual performance-based bonus

  • Benefits Include:

    • Health (Medical, Dental, Vision)

    • Company match 401(k)

    • Employee Stock Purchase Plan (ESPP)

    • Paid Time Off (PTO) & Sick Leave

    • Company car / car allowance (role-dependent)

    • Flexible work-life balance options

Syneos Health complies with federal, state, and municipal regulations regarding paid leave and employee rights.


📊 Role Impact (M23 Level)

Clinical Project Management (CPM) Roles at M23 Level
Are responsible for:

  • Planning, directing, and communicating clinical study timelines

  • Overseeing operational execution of studies across global teams

  • Ensuring consistency and adherence to SOPs, GCP, and regulatory standards

  • Selecting and managing sites and vendors

  • Preparing and tracking clinical trial budgets

  • Developing trial recruitment and delivery strategies

Impact:
Your leadership ensures studies run efficiently, compliantly, and on schedule, directly contributing to successful trial outcomes and the advancement of global research.


🌐 About Syneos Health’s Global Footprint

  • Partnered in 94% of all FDA-approved novel drugs (past 5 years)

  • Supported 95% of EMA-authorized products

  • Delivered 200+ studies across 73,000 sites and 675,000+ patients

🔗 Learn more: www.syneoshealth.com


⚖️ Equal Opportunity Commitment

Syneos Health is an Equal Opportunity Employer.
We value diversity, inclusion, and authenticity and encourage applications even if you don’t meet every qualification.

Transferable skills are welcomed.
We also provide reasonable accommodations under the Americans with Disabilities Act (ADA) for all applicants and employees.


📝 Additional Information

  • Tasks and responsibilities listed are not exhaustive; additional duties may be assigned.

  • Equivalent education or experience will be considered at company discretion.

  • This description does not create an employment contract.

  • Syneos Health is committed to full compliance with all applicable local and international employment laws.


📮 Application Links

🔹 Apply Now: Syneos Health Careers
🔹 Join Talent Network: Stay connected for future opportunities.