Passionate about precision medicine and advancing the healthcare industry?

Summary: 

Responsible for the intake and triage, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) reports according to applicable regulatory guidelines/requirements, Tempus Compass Standard Operating Procedures (SOPs) and project specific instructions.

Independently serves as Lead PVG Associate on complex studies, applying and providing guidance to clients and team members on PVG best practices tailored to the applicable project, patient population, investigational product and client. 

Serves in a mentorship/leadership role with minimal supervision and guidance. 

Job Responsibilities: 

Tasks may include but are not limited to: 

Lead/Perform independently, with minimal guidance and oversight: