Remote Biomarker Study Manager II - Clinical PM

Syneos Health/ inVentiv Health Commercial LLC

Providence (RI)

Remote

USD 95,000 - 176,000

Full time

14 days+
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Benefits offered by this job

Health benefits
401k matching
Company car or allowance
Stock purchase plan
Paid time off and sick time

Job summary

Syneos Health is seeking a Clinical Project Manager II - Biomarker Study Management (Sponsor-Dedicated Remote) to drive biomarker study operations across global trials. You will lead cross-functional teams, vendors, and study partners to ensure biological samples are collected, managed, and analyzed to the highest standards.

The role enables global clinical delivery from start-up to closeout, coordinating sample logistics, timelines, budgets, and regulatory readiness.

Qualifications

  • Significant biomarker study experience with external vendors.
  • Solid understanding of biomarker and bioanalytical strategies in clinical trials.
  • Proven ability to coordinate complex sample collection and analysis workflows.
  • Experience in CRO or sponsor environments; familiarity with GCP/ICH and regulatory standards.

Responsibilities

  • Lead Biomarker Study Operations across Sponsor and Collaborative programs.
  • Serve as operational contact for all biomarker-related processes.
  • Coordinate cross-functional teams, vendors, and internal stakeholders.
  • Plan and manage collection, tracking, and analysis of biological specimens.
  • Ensure TMF accuracy and audit readiness; maintain study systems and data.

Skills

Biomarker studies
Vendors management
Cross-functional coordination
GCP & ICH knowledge
Biomarker strategy
Sample logistics

Education

Bachelor's degree in Life Sciences

Job description

Syneos Health is seeking a Clinical Project Manager II - Biomarker Study Management (Sponsor-Dedicated Remote) to drive biomarker study operations across global trials. You will lead cross-functional teams, vendors, and study partners to ensure biological samples are collected, managed, and analyzed to the highest standards.

The role enables global clinical delivery from start-up to closeout, coordinating sample logistics, timelines, budgets, and regulatory readiness.

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