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

0-2 years

$95,000 – $175,700

Remote, USA

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)
Location: USA – IA – Remote
Updated: November 10, 2025
Job ID: 25102536
Organization: Syneos Health®

🌍 About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success.
With over 29,000 employees across 110 countries, Syneos Health partners with sponsors to design and deliver clinical, medical affairs, and commercial solutions.

Key Facts:

Partnered with 94% of Novel FDA Approved Drugs in the past 5 years
Supported 95% of EMA Authorized Products
Managed 200+ studies across 73,000 sites and 675,000+ patients

Motto: Work Here Matters Everywhere.

💡 Why Work with Us

Career growth & mentorship opportunities
Supportive leadership and therapeutic training
Inclusive Total Self Culture — Be your authentic self
Global diversity and belonging focus
Comprehensive rewards, recognition & development programs

🎯 Position Overview

The Clinical Project Manager II (CPM II) for Biomarker Study Management is responsible for leading global biomarker and bioanalytical operations within sponsor-dedicated clinical trials (Phases I–IV).
This remote role integrates scientific, operational, and project management expertise to ensure successful execution of biomarker studies.

🧠 Key Responsibilities

1. Lead Biomarker Study Operations

Oversee biomarker and bioanalytical activities across sponsor and collaborative programs
Act as primary operational contact for all biomarker-related processes
Integrate biomarker strategies into overall clinical development plans
Manage sample collection, tracking, and analysis workflows
Advise teams on sample logistics and best practices

2. Drive Clinical Project Delivery

Lead cross-functional teams through start-up to closeout
Monitor timelines, budget, scope, and quality compliance
Serve as liaison between sponsors, vendors, and internal teams
Manage project financials and ensure fiscal responsibility
Identify, communicate, and resolve operational risks

3. Ensure Operational Excellence

Maintain Trial Master File (TMF) accuracy and audit readiness
Prepare project reports, dashboards, and sponsor updates
Plan and lead internal/external meetings
Support inspection readiness and regulatory compliance

🧩 Skills & Qualifications

Required:

Proven experience managing biomarker studies and external vendors
Strong understanding of biomarker/bioanalytical strategies in clinical trials
Experience coordinating complex sample management workflows
Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent
Solid knowledge of GCP, ICH guidelines, and global regulations
Excellent project management, communication, and organizational skills
Ability to work independently in a remote setting
Willingness to travel up to 25%

Preferred:

Experience in a CRO or sponsor environment

🚀 What We Offer

Meaningful Impact: Direct contribution to precision medicine and biomarker science
Global Exposure: Work on high-profile international trials
Collaborative Team: Sponsor-dedicated, trusted environment
Remote Flexibility: Structured, supportive virtual work model
Professional Growth: Continuous learning and leadership pathways
Stability: Join a globally respected clinical research organization

💰 Compensation & Benefits

Salary Range: $95,000 – $175,700 (based on experience and qualifications)

Benefits May Include:

Company car or car allowance
Health (Medical, Dental, Vision) benefits
Company-matched 401(k)
Employee Stock Purchase Plan eligibility
Bonus or commission opportunities
Flexible PTO and sick leave (state-regulated variations apply)

🧾 Additional Information

Duties are not exhaustive and may evolve per company needs.
Equivalent experience/education will be considered.
Syneos Health is an Equal Opportunity Employer, compliant with ADA and EU Equality Directive standards.
Reasonable accommodations are available upon request.

📅 Core Functional Focus

Clinical study planning & timeline management
Operational oversight & consistency across studies
Compliance with SOPs, GCP, and country regulations
Site & vendor selection
Budget preparation & financial tracking
Recruitment strategy development
Progress monitoring and team follow-up
Implementation of clinical development strategies

🌟 Impact

This role significantly influences the success and integrity of clinical trials, ensuring that biomarker-driven research meets scientific, operational, and regulatory standards—ultimately accelerating innovation in clinical development.

🔗 Learn More: www.syneoshealth.com
📩 Apply Now: Join a mission-driven global organization shaping the future of clinical research.
🌐 Talent Network: Not ready to apply? Join our Talent Network to stay connected.

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

Job Description

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