
Senior Clinical Documentation Specialist
3 days ago
Delhi and Bangalore are the primary locations for this role.
- We require a skilled professional to develop high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
- The ideal candidate will be able to translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
- Additionally, they should have strong scientific communication skills, as demonstrated by their ability to craft abstracts and manuscripts.
- The successful candidate will deliver high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
- Key responsibilities include preparing protocols, CSRs, PIS-ICFs, and CRFs, understanding study objectives, designing protocols, and reviewing SOPs.
- Effective communication with all stakeholders is crucial to ensure timely and complete documentation.
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Clinical Trial Document Specialist
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Documentations Specialist
3 days ago
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Clinical Systems Specialist Position
2 days ago
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