Description
Requirements- M.S. or Ph.D. in a scientific discipline
- Minimum seven (7) years of medical writing, preparing clinical protocols, IBs, abstracts, manuscripts and reviews for clinical trials for biotech/pharmaceutical companies.
- Experience writing CSRs for pivotal/registration studies or writing clinical sections of licensing submissions essential. NDA submission experience preferred.
This Job presents the opportunity to work side by side with researchers on the forefront of progressive biopharmaceutical research with a leading company in the industry
If you would like to be considered for an interview please contact me, and send over an updated resume.