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Clinical Bio-Sample Operations Manager (Clinical Trials) #3556805
Bridgewater, NJ
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Be Part Of A High-Performing Team

This opportunity is with a growing biotechnology organization advancing innovative therapies across rare diseases and emerging therapeutic areas. The clinical operations team is rapidly expanding to support an increasing pipeline of studies, including large-scale global trials.

The environment is fast-paced and highly collaborative, bringing together clinical operations, development, biometrics, and laboratory partners. This role sits at the center of that ecosystem—owning the operational execution of biospecimen and laboratory workflows across multiple clinical programs.

What's In Store For You

Engagement: W2 only (no C2C/1099)

  • Opportunity to support high-impact clinical trials across multiple phases and therapeutic areas
  • Work in a fast-growing organization with expanding clinical programs
  • Exposure to cross-functional collaboration across global clinical teams and laboratory partners
  • Opportunity to take ownership of critical operational workflows tied to clinical trial success
  • Remote flexibility (preference for East Coast alignment due to team collaboration)

How You Will Make An Impact

  • Serve as the operational lead for biospecimen and laboratory activities across clinical trials
  • Partner closely with Clinical Trial Managers and study teams to ensure sample strategies align with protocol requirements
  • Oversee central and specialty laboratory vendors with a focus on day-to-day operational execution
  • Ensure biospecimens are collected, processed, shipped, and tracked in compliance with protocol and lab manuals
  • Monitor chain-of-custody and perform real-time tracking and reconciliation of samples across systems
  • Review protocols, ICFs, and study documents to ensure sample requirements are clearly defined and executed
  • Manage sample tracking tools and reconcile data across EDC systems, lab databases, and CRO outputs
  • Investigate and resolve sample discrepancies, lost samples, and data inconsistencies
  • Support clinical sites with training and guidance on sample collection and handling procedures
  • Coordinate across internal and external stakeholders to ensure timely sample delivery and data integrity
  • Contribute to process improvements and SOP development related to biospecimen operations
  • Support multiple studies simultaneously, including large-scale Phase II/III trials 


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