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About the Role
- 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.
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