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US 5w PTO

  • Lead global pharmacovigilance operations and ensure the safety of clinical and post-marketing products.
  • Collaborate with cross-functional teams to maintain compliance with global regulatory standards.
  • Drive continuous improvement of PV systems and processes while contributing to medical safety strategy.

GCP ICH Microsoft Office

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$325,000–$376,000/yr

  • 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.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease.