Senior Director, Pharmacovigilance
- Lead Braveheart’s global PV strategy and partner closely with Clinical, Regulatory, and other development functions.
- Lead all PV contributions to Investigational New Drug (IND) and Clinical Trial Application (CTA) submissions worldwide, with responsibility for developing high-quality safety sections.
- Shape the future PV function— its people, structure, and operating model— as Braveheart transitions from clinical development to post-market commercialization.
$325,000–$376,000
/yr