Freelance Clinical Medical Writer
transperfect4 · Delhi
Job description
About the role
We are expanding our pool of freelance medical writers to support client projects that require high‑quality clinical documentation. The role focuses on creating and reviewing key trial documents for pharmaceutical and biotech studies.
Key responsibilities
- Develop and write clinical trial protocols.
- Prepare comprehensive clinical study reports.
- Draft informed consent forms for study participants.
- Create investigators' brochures and related materials.
Required profile
- Based in India.
- Excellent written and verbal communication skills in English.
- Science degree (e.g., life sciences, pharmacy, or related field).
- Minimum 5 years of experience as a Clinical Medical Writer.
Required skills
- Specialized knowledge of clinical trial protocols, study reports, informed consent forms, and investigators brochures.
- Acute attention to detail, spelling and grammar.
- Ability to maintain professionalism under tight deadlines.
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Published 2 weeks ago
Expires 1 month from now
31 views · 0 interested
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transperfect4
Delhi