Contract Associate Director of Regulatory Affairs
Contract - One Year
My client is a midsize international pharmaceutical company focused on innovative treatments for oncology and endocrine disorders. This growing pharmaceutical company has multiple studies in phase 1-3. The team is looking to bring on a fully remote Associate Director of Regulatory Affairs.
Associate Director of Regulatory Affairs will be responsible for:
- Developing regulatory strategies and plans across global teams
- Contributing to development of labeling documents across international markets
- Manage and prepare complex regulatory submissions
- Propose and identify strategies to mitigate risk
- Responsible for monitoring activities or direct reports in addition to own tasks
The Associate Director of Regulatory Affairs should have the following qualifications:
- 10+ years of Regulatory Affairs Experience
- Dossier filing experience including IMPDs, INDs, and CTAs
- Bachelor's Degree or higher in a scientific discipline
- Experience implementing regulatory strategies for CMC, clinical, and non-clinical
If you are interested in the Associate Director of Regulatory Affairs position, then please don't wait to apply!