Trainee - Medical Reviewer

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.