Internal Medicine Physician

Epic Staffing Group

Not Specified, Connecticut, United States

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Ensure the medical safety of study participants.
Oversee site personnel in the execution and delivery of safe trial practices.
Review and report on screening failures, safety and participant retention rates.
Oversee clinical evaluation and assessments of clinical trial studies.
Interface with IRBs and study Sponsors on a regular basis.
Comply with all medical duties per study protocols, SOP, GCP and state regulations.
Collect and analyze data to identify patterns or trends of the clinical trials.
Prepare detailed reports documenting findings and recommendations for improvement.
Stay up-to-date with the latest developments in SOPs and documentation requirements.