This is a contract role for a Principal Investigator.
The Principal Investigator will be responsible for overseeing the conduct of clinical trials, ensuring adherence to the protocols. This is a hybrid role, with an occasional office visit.
Qualifications
Experience as a Principal Investigator or Sub-Investigator in clinical trials
Knowledge of FDA regulations and Good Clinical Practice (GCP) or a willingness to learn
Excellent written and verbal communication skills
Ability to work independently and as part of a team
Strong organizational and time-management skills
MD or DO, Board certification is a plus
Licensed in the State of SC