U.S.- based remote role - preference for CST/EST candidates
Bonus and L.I.T. eligible incl. hire on RSUs/Options
Global medical device client focused on Oncology treatments seeks a Regulatory specialist to provide expertise and support for it's regulatory pathways including strategies around product development, regulatory submissions, clinical studies, and internal policy and procedure development.
REQUIREMENTS:
- Law degree
- 5+ years of Life Sciences related Regulatory experience, either internal or as external counsel
- Significant experience with Class III medical devices, or drug/biologics regulatory regulations
- Demonstrated experience with preparing and submitting to FDA, both pre- and post-market submissions
- Excellent written and verbal communicator