Added
5 days ago
Type
Full time
Salary
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Related skills

risk management gcp stakeholder management vendor management budgeting

📋 Description

  • Provide end-to-end operational leadership for clinical studies from start-up through close-out and
  • Identify study/program risks and escalate site, vendor, and operational issues with mitigation
  • Develop and own study-level operational plans including monitoring, vendor oversight, risk
  • Lead feasibility, site selection, and enrollment planning using data-driven approaches.
  • Forecast resources across internal teams and CROs to ensure staffing and coverage.
  • Manage study budgets, forecasts, and change orders with Finance and leadership.

🎯 Requirements

  • Bachelor’s degree in Life Sciences or related field or equivalent experience.
  • At least 8 years of clinical experience in pharma/biotech with increasing responsibility.
  • At least 2 years of clinical project management with ownership of study delivery.
  • Strong understanding of clinical operations, including planning, site management, monitoring
  • Solid knowledge of ICH/GCP, clinical research standards, and regulatory requirements.
  • Demonstrated ability to lead cross-functional teams and manage CROs/vendors; data-driven with

🎁 Benefits

  • Competitive salary range of $125,000–$170,000, depending on qualifications and experience.
  • Opportunity to contribute to innovative approaches to neuroscience and mental health.
  • Collaborative, cross-functional environment with opportunities to lead clinical programs.
  • Inclusive workplace committed to kindness, empathy, respect, and equal opportunity.
  • Potential flexibility around remote work depending on role and circumstances.
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