North AmericaFull TimeOperations
Remotely
gcpclinical operationsrisk managementvendor managementstakeholder managementcrobudgetingdata driven
Job Description
📋 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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