Description
Desired Experience- Advanced degree such as a PhD, MD, or DVM and will have demonstrated training and/or expertise in oncology research or a closely-related biological science.
- More than 10 years experience in both early and late stage drug development with emphasis on authoring expert nonclinical summary documents.
- Have authored pharmacology/toxicology sections for a significant number of INDs and preferably 1-2 BLAs or NDAs.
- Regulatory expertise in non-clinical pharmacology- Ability to assess appropriate response to regulatory requests/queries.
This position provides to work with one of the global leaders in pharmaceutical development and contribute to groundbreaking work within oncology.