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

0-2 years
$95,000 – $175,700 (USD)
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 leading integrated biopharmaceutical solutions organization focused on accelerating customer success by combining clinical, medical, and commercial expertise.

Our mission is to bring patients and customers to the center of every decision we make — streamlining clinical development and delivering therapies that change lives.

With 29,000 employees across 110 countries, Syneos Health drives innovation, collaboration, and performance excellence in every stage of biopharmaceutical development.

Motto: WORK HERE MATTERS EVERYWHERE


🌟 Why Work at Syneos Health

  • Career Development: Comprehensive growth opportunities through mentorship, training, and internal mobility.

  • Supportive Culture: Engaged leadership, technical training, and peer recognition.

  • Authentic Work Environment: Our Total Self culture encourages employees to be their true selves.

  • Diversity & Inclusion: We value diverse perspectives, backgrounds, and experiences to foster belonging.

  • Recognition & Rewards: Competitive total rewards package and flexible work-life balance.


🧠 Position Overview

The Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote) plays a vital role in managing biomarker and bioanalytical study operations within global clinical trials.

You will lead cross-functional teams, vendors, and stakeholders to ensure efficient collection, tracking, and analysis of biological samples, driving project success from start-up to closeout.

This is a fully remote, sponsor-dedicated opportunity ideal for professionals with experience in biomarker operations, bioanalytics, and clinical project management.


🔧 Key Responsibilities

1️⃣ Lead Biomarker Study Operations

  • Oversee biomarker and bioanalytical activities across sponsor and collaborative programs.

  • Act as the primary operational point of contact for all biomarker-related processes.

  • Collaborate with clinical study teams (Phases I–IV) to integrate biomarker strategies into study design.

  • Plan and manage collection, tracking, and analysis of biological specimens.

  • Advise teams on best practices for sample logistics and operational workflows.

2️⃣ Drive Clinical Project Delivery

  • Manage cross-functional teams throughout the clinical trial lifecycle.

  • Ensure projects remain within defined timelines, budgets, scope, and quality metrics.

  • Serve as the liaison between sponsors, CROs, and vendors.

  • Monitor and control project financials, identifying risks and corrective actions.

  • Facilitate proactive issue resolution to maintain study performance.

3️⃣ Ensure Operational Excellence

  • Maintain complete and accurate documentation, ensuring Trial Master File (TMF) compliance.

  • Keep systems and databases audit-ready and up to date.

  • Prepare detailed reports and updates for sponsors and internal stakeholders.

  • Lead team meetings and ensure inspection readiness per GCP and regulatory standards.


🧩 Required Skills & Experience

Qualification Area

Requirement

Education

Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or related field

Experience

Proven background in managing biomarker studies and working with external vendors

Technical Expertise

Strong understanding of bioanalytical and biomarker operations in clinical settings

Project Management

Ability to coordinate complex workflows and multi-site clinical studies

Regulatory Knowledge

Familiar with GCP, ICH, and global regulatory compliance

Tools & Systems

Skilled in clinical systems, project reporting, and documentation tools

Soft Skills

Excellent communication, organization, problem-solving, and leadership skills

Work Setup

Comfortable working independently in a remote, fast-paced environment

Travel

Up to 25% as required


🌍 Why Join Syneos Health

  • 💉 Meaningful Work: Directly contribute to advancing precision medicine and biomarker science.

  • 🌎 Global Reach: Manage multi-regional clinical studies impacting patient outcomes globally.

  • 👥 Collaborative Team: Join a sponsor-dedicated group that values innovation and expertise.

  • 🏡 Remote Flexibility: Enjoy full work-from-home freedom with strong organizational support.

  • 🚀 Growth Opportunities: Continuous learning and leadership development programs.

  • 🏢 Stability & Reputation: Partner with a trusted leader in global clinical research.


💵 Compensation & Benefits

Salary Range: $95,000 – $175,700 (USD)

Final pay determined by skills, experience, and qualifications.

Benefits Package Includes:

  • Medical, Dental, and Vision insurance

  • 401(k) with company match

  • Employee Stock Purchase Plan

  • Performance-based bonus or commission eligibility

  • Company car or car allowance (where applicable)

  • Flexible Paid Time Off (PTO) and regulated sick leave

  • Work-life balance and quality-of-life initiatives


🧬 About Syneos Health – Global Impact

Over the last 5 years, Syneos Health has:

  • Partnered on 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

  • Job responsibilities are not exhaustive; duties may evolve based on business needs.

  • Equivalent education or experience may substitute formal qualifications.

  • Syneos Health is an Equal Opportunity Employer committed to ADA compliance and reasonable accommodations.

  • Employment terms do not create a contractual obligation.


🧭 Role Summary (M23 Level – Clinical Project Management)

Core Responsibilities

  • Plan, direct, and communicate clinical study timelines.

  • Oversee operational aspects of global clinical trials.

  • Ensure adherence to SOPs, GCP, and regulatory standards.

  • Conduct site and vendor selection and manage trial budgets.

  • Monitor project progress and support clinical development strategy.

  • Develop and execute recruitment strategies.

Impact & Contribution

This role significantly impacts the success of clinical trials by ensuring timely execution, quality outcomes, and regulatory compliance — driving the integrity and advancement of global research.


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