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Clinical Research Associate

0.00 to 2.00 Years   Hyderabad   17 Jan, 2023
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaPharmacist / Medical Representative
EmploymentTypeFull-time

Job Description

    Roles and Responsibilities of CRA:
    • Identifying/selecting an investigator who will be responsible for the conduct of the trial at the trial site.
    • Liaising with doctors/consultants or investigators on conducting the trial.
    • Setting up the trial sites, which includes ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product. Training the study staff in standard operating procedure for the clinical trials as per applicable regulatory requirements.
    • Verify that investigator and investigators team are adequately trained and comply with the protocol.
    • Verify that IRB/IEC operates and complies as per GCP, SOP and applicable regulatory requirements.
    • Monitoring the trial throughout specified duration involving monitoring visit to the trial sites.
    • Source data verification
    • Informed consent form review, case report form review, investigational drug accountability, and adverse event review.
    • Ensuring all unused trial supplies are accounted for. Writing visit reports, filing and collecting trial documentation and reports.

Keyskills :
clinical trialsclinical researchclinical trial management systemclinical monitoring

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