Medical Writer
Job Location:
Remote (India)
Experience:
2-4 years of experience as Regulatory medical writing in clinical trials
Qualification:
M. Pharm – Pharmacology/ Pharma D
Job Responsibilities:
- Prepare clinical/regulatory documents: protocols, CRFs, IB, Module 2 docs, CSRs, SAPs
- Scientific writing for publications, posters, SEC presentations
- Collaborate with PM, Biostatistics, Medical Monitor; manage timelines and QMS compliance