Clinical Research Internship

Selected intern's day-to-day responsibilities include:

1. Identifying/selecting an investigator who will be responsible for the conduct of the trial at the trial site
2. Liaising with doctors/consultants or investigators on conducting the trial
3. Setting up the trial sites, which includes ensuring each center has the trial materials, including the trial drug often known as the investigational medicinal product Training the study staff in the standard operating procedure for the clinical trials as per applicable regulatory requirements
4. Verifying that the investigator and the investigator s team are adequately trained and comply with the protocol
5. Verifying that IRB/IEC operates and complies as per GCP, SOP, and applicable regulatory requirements
6. Monitoring the trial throughout a specified duration involving monitoring visits to the trial sites
7. Sourcing data verification
8. Working on informed consent form review, case report form review, investigational drug accountability, and adverse event review
9. Ensuring all unused trial supplies are accounted for
10. Writing visit reports, filing and collecting trial documentation and reports

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