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

Remote / Online - Candidates ideally in
Oregon, Dane County, Wisconsin, 53575, USA
Listing for: Syneos Health, Inc.
Remote/Work from Home position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 95000 USD Yearly USD 95000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote)

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

Updated: November 10, 2025

Location: USA-OR-Remote

Job :

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

Job Responsibilities 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 processes
  • Work closely with clinical study teams (Phases 1-4) to integrate biomarker strategies into broader clinical development plans
  • Plan and manage the collection, tracking, and analysis of biological specimens
  • Advise study teams on best practices for sample management and logistics
Drive Clinical Project Delivery
  • Lead cross‑functional teams through the full clinical trial lifecycle, from start‑up to closeout
  • Ensure studies stay on track with respect to timelines, budget, scope, and quality
  • Act as the main liaison between the sponsor and study partners
  • Monitor and manage project financials, ensuring fiscal responsibility
  • Proactively identify and resolve operational issues and risks
Ensure Operational Excellence
  • Maintain high‑quality documentation, including Trial Master File (TMF) accuracy and completeness
  • Keep study systems and databases current and audit‑ready
  • Prepare project reports and updates for sponsors and internal stakeholders
  • Plan and facilitate internal and external meetings
  • Support inspection readiness and regulatory compliance throughout the project
Skills and Experience You Bring
  • Significant experience managing biomarker studies and external vendors
  • Strong understanding of biomarker and bioanalytical strategies in a clinical trial setting
  • Proven ability to coordinate complex sample collection and analysis workflows
  • Expertise in supporting study teams with sample logistics and operational planning
  • Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience
  • Experience in a clinical research organization (CRO) or sponsor environment preferred
  • Familiarity with GCP, ICH guidelines, and global regulatory standards
  • Strong project management, organizational, and communication skills
  • Comfortable working independently and embracing new technologies
  • Willingness to travel up to 25% as needed
Benefits
  • Company car or car allowance
  • Health benefits:

    medical, dental, and vision
  • Company match 401(k)
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO) and sick time
Salary Range

$95,000.00 – $

Salary will vary based on qualifications, skills, competencies, and proficiency for the role.

Apply Now

If you’re passionate about clinical research and want to make a direct impact on advancing biomarker science, we’d love to hear from you.

At Syneos Health, we believe in providing an environment and culture in which our people can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality‑of‑life balance.

Equal Opportunity Employer

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at:

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