Posted:2 weeks ago|
Platform:
Work from Office
Full Time
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, pharmacovigilance, 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.
Omega Healthcare
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