The Manager, Clinical Operations will ensure excellence in clinical trial planning, execution, and data collection, in accordance with regulatory guidelines, and will be responsible for aspects of clinical study conduct, including site selection, study start-up, conduct and close-out.
Requirements
- Manage multiple aspects of clinical studies
- Perform oversight of CRO and auxiliary vendors
- Provide support and oversight managing the creation, maintenance and close out of TMF activities
- Ensure site monitoring reports are accurate and thorough
- Support database lock by ensuring appropriate oversight of sites and by participating in data review/reconciliation efforts
- Coordinate with Clinical Supply Chain regarding drug forecasting and supply of drug product to sites
Benefits
- Medical, dental, and vision insurance
- 401(k) retirement savings plan
- Generous paid time off (including a summer and winter company shutdown)
- Other benefits (not specified)