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Specialist Document Coordinator-Quality Reviewer for Regulatory and Safety Documents Merck Group

2.0 - 6.0 years

0 Lacs

karnataka

On-site

Role Overview: You will be joining as a Senior Associate/Specialist Document Coordinator, supporting the Global Medical Writing Team in delivering its portfolio effectively and efficiently. Your main responsibilities will include managing the quality review of clinical and regulatory documents, such as Protocols, Clinical Study Reports, Briefing Books, Investigator Brochures, Clinical Summary documents, PBRER, DSUR, and RMP. Key Responsibilities: - Conduct quality review of clinical and regulatory documents - Participate in meetings related to medical writing, quality control, and compliance activities - Collaborate cross-functionally to continuously improve medical writing processes - Famil...

Posted 2 months ago

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