Scientific Writer II
HyderabadFull-timeMid levelPosted 5 days ago
Closed
Mid-level content and media role at Transform Your Career Journey at Bristol Myers Squibb | Explore Open in Hyderabad. Needs an M.Pharm or PhD.
About the role
Coordinate and author regulatory documents [eg, Investigator's Brochures (IB), development safety update reports, periodic benefit-risk evaluation reports, clinical study reports (CSR), and protocols] ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members.
What you'll do
- Coordinate and author regulatory documents [eg, Investigator's Brochures (IB), development safety update reports, periodic benefit-risk evaluation reports
- Participate in relevant document subteam(s) and ensure effective planning and management of timelines for all components of assigned documents
- Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects
- Maintain document prototypes and shells
- Review and edit documents as required
What you need
- Writing
- Prototyping