Principal Medical Writer - Regulatory Submission D

• Bachelor's degree in a relevant discipline with relevant writing experience; graduate degree preferred
• 3-5 years of relevant experience in science, technical, or medical writing
• Experience working in the biopharmaceutical, device, or contract research organization industry required
• Experience writing relevant document types required

Overview

• Industry - IT - Software / Product Development
• Functional Area - Doctors / Medical Professionals / Clinical Research / Pharma Medical Affairs
• Job Role - Other Clinical Research / Clinical Trials / Clinical Data Management / Pharmacovigilence
• Employment type - Full Time
• Work Mode - Remote

Qualifications

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

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