The Sub-Investigator I is responsible for supervising clinical activities for the clinical trial to which they are assigned. The Sub-Investigator I will promote Good Clinical Practices (GCP) during the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to regulation/guidance and standard operating procedure (SOP).
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree