Skip to main content
Locations: Princeton, NJ; San Diego, CA; or San Francisco, CA
Schedule
Hybrid: 3 days/week onsite
We are representing a senior-level Clinical Operations opportunity with one of our clients. This is not a role at GQR. The client is looking for a strong study leader who can drive end-to-end execution of Phase 2-4 clinical trials, partner across cross-functional teams, and oversee vendors while maintaining high standards for quality, compliance, and timelines. This individual will play a central role in study delivery, from startup through closeout, and will be expected to bring a proactive, solutions-oriented approach in a fast-paced environment.
Key responsibilities include:
  • Leading study execution across startup, enrollment, conduct, and closeout
  • Managing cross-functional teams and external vendors
  • Owning timelines, budgets, study plans, and operational deliverables
  • Supporting inspection readiness and ongoing compliance efforts
  • Providing regular updates to leadership and project stakeholders
  • What the client is looking for:
  • Bachelor’s degree in life sciences or related field 5+ years in clinical trial management
  • In-house pharma or biotech experience preferred
  • Strong sponsor-side study management background
  • Manager-level experience, ideally 3-4+ years at that level
  • Broad technical depth across clinical operations
  • Rare disease experience is a plus
Compensation: Base salary of $131,000-$163,600 for the right profile, plus bonus/equity potential.

Matching similar jobs

Level

Senior L5

Salary

$131,000 per year

Location

San Diego, CA

Occupation

Project Management Specialists

Industry

Research and Development in Biotechnology

Posted

yesterday

APPLY NOW (opens in a new tab)