15 Oct
|
Excelra
|
Hyderabad
Roles and Responsibilities :
- Review and edit clinical trial reports, protocols, and other documents to ensure accuracy, completeness, and compliance with regulatory requirements.
- Collaborate with cross-functional teams to develop high-quality scientific content for pharmaceutical companies.
- Conduct thorough research on various medical topics to stay up-to-date on industry trends and best practices.
- Ensure all edited materials meet client expectations by providing timely feedback and revisions.
Job Requirements :
- 5-8 years of experience in medical writing or editing for the pharmaceutical industry.
- Robust understanding of clinical trials, drug development processes, and regulations (e.g., FDA guidelines).
- Excellent written communication skills with ability to adapt tone and style according to audience needs.
- Proficiency in using electronic health records systems (EHRs) or similar software.
📌 Editor AI (Hyderabad)
🏢 Excelra
📍 Hyderabad