Biomarker Study PM II – Remote, Sponsor-Dedicated

Syneos Health, Inc.

California (MO)

Remote

USD 110,000 - 150,000

Full time

2 days ago
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Benefits offered by this job

Company car or car allowance
Health benefits
401k match
Employee stock purchase plan
Paid time off and sick time

Job summary

Syneos Health, Inc. is seeking a Clinical Project Manager II with biomarker study operations expertise for a sponsor-dedicated, remote US role with a preference for hybrid Foster City, CA.

You will lead cross-functional teams to ensure sample collection, analysis, and regulatory compliance across global trials. Ideal candidates will have strong biomarker trial experience, GCP/ICH knowledge, and excellent communication and organizational skills.

Qualifications

  • Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent.
  • Experience in CRO or sponsor environment preferred.
  • Familiarity with GCP, ICH guidelines, and global regulatory standards.
  • Strong project management, organizational, and communication skills.
  • Willingness to travel up to 25%.

Responsibilities

  • Lead Biomarker Study Operations
  • Oversee biomarker and bioanalytical activities across Sponsor and Collaborative programs
  • Serve as operational contact for biomarker processes
  • Work with study teams to integrate biomarker strategies
  • Plan and manage collection, tracking, and analysis of biological specimens
  • Advise on sample management and logistics

Skills

Biomarker studies
Biomarker study operations
Cross-functional collaboration
Sponsor/dedicated execution
GCP & ICH knowledge
Project management
Communication skills
Travel 25% willingness

Education

Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing

Job description

Syneos Health, Inc. is seeking a Clinical Project Manager II with biomarker study operations expertise for a sponsor-dedicated, remote US role with a preference for hybrid Foster City, CA.

You will lead cross-functional teams to ensure sample collection, analysis, and regulatory compliance across global trials. Ideal candidates will have strong biomarker trial experience, GCP/ICH knowledge, and excellent communication and organizational skills.

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