- Must have strong phase IV and/or post-market study experience
- Virology, Oncology, or rare disease experience is preferred
- Demonstrated ability to manage and experience of Post-Authorisation (PAS) Non-Interventional studies and clinical trials including PASS/PMR globally
- Collaboration with colleagues in Clinical Operations, Medical Affairs, Pharmacovigilance & Epidemiology, Project Management, Regulatory, Biometrics and Clinical Research globally ensuring delivery of assigned studies
- Ensures the successful management of activities across multiple therapy areas through teams and the appropriate use of internal and external resources (ARO/CRO)
- Experience of Investigator Sponsored Research (ISR) including Fair Market Value and feasibility assessment, contract negotiation support, tracking and publication follow-up
- May support/oversee Compassionate Use programs
- Member of Global Late Phase Leadership Team responsible for the effective delivery of Late Phase accountabilities
- Manages people managers and/or study teams to ensure optimal deployment of resources
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Director, Clinical Operations - Late Phase
- Location San Francisco
- Job type Permanent
- Salary Negotiable
- Discipline Clinical Operations
- Reference PR/314036_1628880454