Description
Job 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 position offers the opportunity for an individual to work in one of the leading biopharmaceutical companies in the industry alongside some of fields most innovative individuals.
If you would like to be considered for an interview please contact me, and send over an updated resume.