Medical Writer II

December 5

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Description

• Responsible for management of scheduled and unscheduled aggregate reports. • Performing aggregate report compliance activities including quality review. • Coordinating with the members of Study Management Team to discuss formats and templates.

Requirements

• Relevant experience is desirable in Regulatory/ Pharmacovigilance or related field. • Good knowledge of medical terminologies