- Remote, India
- Remote
- Full-time
- 2+ years
Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
Responsibilities
- Serve as primary author for routine documents such as clinical study reports and study protocols
- Summarize data from clinical studies
- Assist with complex clinical and scientific program level documents including IBs, INDs, and MAAs
- Ensure compliance with quality processes and requirements
- Assist in determining best practices, methods and techniques for optimal results
Requirements
- Bachelor's degree in a scientific discipline or equivalent
- Nice to have: experience in pharmaceutical/CRO industry
- Nice to have: experience in scientific writing