Trainee - Medical Reviewer

3 - 5 years

3 - 5 Lacs

Posted:1 week ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Key Responsibilities:

  • Review and assess medical documents, including clinical trial data, safety reports, and regulatory submissions, for accuracy, consistency, and compliance with industry standards.
  • Assist in the preparation of regulatory documents, such as clinical study reports, informed consent forms, and patient safety reports.
  • Ensure that all content aligns with medical and scientific guidelines, including Good Clinical Practice (GCP) and regulatory requirements.
  • Collaborate with senior medical reviewers and other cross-functional teams (e.g., clinical research, pharma co-vigilance, regulatory affairs) to ensure the timely and accurate delivery of medical documents.
  • Review medical literature and stay updated on the latest clinical and scientific research relevant to assigned projects.
  • Identify and flag potential issues or discrepancies in clinical trial data or reports.
  • Assist in the preparation of training materials or presentations related to medical review processes.
  • Support senior medical reviewers in maintaining high standards of medical and scientific integrity.

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