Clinical Research Physician Micro Crispr Pvt. Ltd.

3.0 - 5.0 years

0 Lacs

ahmedabad, gujarat, india

On-site

Medical Oversight Provide ongoing medical monitoring of assigned clinical trials, including real-time safety review of adverse events (AEs) and serious adverse events (SAEs). Evaluate safety signals, trends, and laboratory/ECG abnormalities to ensure participant well-being. Assess investigator-reported causality and provide independent medical judgment when required. 2. Protocol Development and Study Design Contribute to clinical protocol writing, amendments, and study-related documents (IB, CSR, SAP). KOL engagement Ensure protocol design is scientifically rigorous, ethical, and aligned with regulatory expectations. Participate in the development of informed consent forms and patient inform...

Posted 5 days ago

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Medical Reviewer Vipany Management Consulting

3.0 - 7.0 years

4 - 9 Lacs

hyderabad

Work from Office

We are seeking an experienced and detail-oriented Medical Reviewer to join our team. The role involves reviewing, analyzing, and ensuring accuracy, consistency, and compliance of medical and scientific content in alignment with regulatory, clinical, and organizational standards. Key Responsibilities Review medical, clinical, and regulatory documents for scientific accuracy, clarity, grammar, and compliance. Ensure consistency of terminology, data, and style across all documents. Validate clinical and safety data in reports and submissions against source documents. Collaborate with cross-functional teams including medical writers, clinical research, and regulatory affairs. Provide feedback an...

Posted 3 months ago

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