Associate, medical writer

• Prepares, with supervision, written clinical documents including clinical study reports according to applicable GCP requirements, regulatory requirements, and guidance documents (including but not limited to ICH E3 guidelines and company SOPs).

Overview

• Industry - CRO, Clinical Research Organization
• Functional Area - Pharmacovigilence / Clinical Research
• Job Role - Documentation/Medical Writing
• Employment type - Full Time - Permanent
• Work Mode - Remote

Qualifications

• Any Graduate - Any Specialization
• Any Post Graduate - Any Specialization
• Any Doctorate - Any Specialization

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