Offer summary
Qualifications:
Bachelor's degree in scientific discipline, Advanced degree preferred, Experience as a writer (2-5 years) or equivalent combination, Knowledge of global regulatory guidelines, Previous experience in pharmaceutical/CRO industry preferable.
Key responsabilities:
- Research, write, and edit clinical study reports, protocols
- Manage projects independently, interact with various departments
- Represent department in client interactions
- Assist with business development and proposals