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Senior Regulatory Operations Associate
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- Passionate about precision medicine and advancing the healthcare industry?
- The Senior Regulatory Operations Associate provides trial support to the Regulatory Operations team and Regulatory Affairs and Investigator Services department, thereby contributing to the overall management of clinical trials in accordance with applicable regulatory guidelines/requirements, Tempus Compass Standard Operating Procedures (SOPs) and project specific plans.
- Job Responsibilities: Completes applicable protocol and disease indication training as needed.
- Uploads documents to the Trial Master File (TMF).
- Maintains site tracking in Clinical Trial Management Systems (CTMS), as applicable for the lifetime of the study.
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