Clinical Trial Operational Manager
Cambridge, MA, United States On-site
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About the role
The CTOM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, observational studies, compassionate use and registries) including data management activities in compliance with GCP s, SOPs and standards within established timelines and budgets. The CTOM is involved in the scientific conduct of the study and acts as the leader of operational disciplines to guarantee release of homogeneous high quality data, in close collaboration with other CSO department representatives (e.g. Medical Operations) May be required to take-on the Dedicated Project Expert (DPE) role depending on CTOM s level of experience, relevant skill-set and business needs.
What you'll bring
- advanced degree preferred