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Tuesday, 1 October 2013

Clinical Research Associate Bharat Biotech - Hyderabad..."R"

Clinical Research Associate
Bharat Biotech - Hyderabad, Andhra Pradesh
Ethics Committee submissions/DCG(I) submissions.
  • Visits like Site Evaluation, Site Initiation, Interim Monitoring visit and Study close-out visit.
  • Following up on previously identified issues like Informed Consent, outstanding corrections on forms and missing documents in Regulatory files.
  • Clinical Trial Updates from all the sites and addressing to the core issues.
  • Maintaining Trial Master File (TMF).
  • Preparing Clinical Trial Documents including Investigator Brochure, Clinical Trial Agreements, PSURs (Periodic Safety Update Report).
  • Preparation of SOPs.
  • Verification of eligibility of subjects being enrolled by the Investigator.
  • IP (Investigational Product) review and accountability.
  • Answering to DCG (I) queries/Site queries.
  • Designing PMS Forms & Informed Consent Forms.
  • Qualification: MBBS/MD
    Experience: 0-10 Yrs
    Job Reference Code: BB/CRA/001
    Salary as per company normsclick here to view /apply

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