Global Senior Clinical Trial Lead

Praxy

Northern (KY)

Hybrid

USD 120,000 - 180,000

Full time

2 days ago
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Job summary

Bicara Therapeutics is seeking a Senior Clinical Trial Manager to lead and oversee multi-region clinical trials, ensuring high standards of quality and compliance. You will drive vendor oversight, site performance, and risk management while partnering with cross-functional teams, sites, and CROs to execute trials efficiently.

The role requires a strong background in clinical operations, global trial management, and preferably Phase 2/3 and oncology experience.

Qualifications

  • Bachelor’s degree in life sciences is required.
  • Minimum of 5 years’ clinical trial management experience in pharma/biotech/CRO.
  • Experience managing global trials across geographies and regulatory regimes.
  • Phase 2/3 experience and oncology exposure are strongly preferred.
  • Operational knowledge, project planning, and oversight of CROs/vendors.

Responsibilities

  • Oversee day-to-day management of one or more clinical trials across regions.
  • Partner with cross-functional teams, sites, and CROs to ensure study quality and timelines.
  • Drive vendor oversight, site performance, risk management and issue resolution.
  • Develop or revise study documents and ensure regulatory and quality standards.
  • Monitor progress, budgets, and timelines; manage CROs and third-party vendors.
  • Contribute to regulatory documents and study-related publications as needed.

Skills

Clinical operations management
Vendor oversight
Cross-functional collaboration
Regulatory compliance

Education

Bachelor's degree in Life Sciences

Tools

Clinical trial software

Job description

Bicara Therapeutics is seeking a Senior Clinical Trial Manager to lead and oversee multi-region clinical trials, ensuring high standards of quality and compliance. You will drive vendor oversight, site performance, and risk management while partnering with cross-functional teams, sites, and CROs to execute trials efficiently.

The role requires a strong background in clinical operations, global trial management, and preferably Phase 2/3 and oncology experience.

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