Senior Director, Drug Safety (GK)

Date Posted: 2/14/2023 12:09:59 PM

Senior Director, Drug Safety
Boston, MA (hybrid)

Clark Davis is partnered with multiple pharmaceutical companies to support the build out of their Drug Safety departments. We are actively recruiting for Senior Directors across multiple therapeutic areas, including Oncology and Rare Disease among others. These roles are all hybrid reporting to offices in Boston, MA, Northern NJ, or Northern California.

Responsibilities:
Safety surveillance for pharmaceutical / biological products. Lead strategy initiatives and write the key pharmacovigilance documents. Understanding and application of pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. Apply current regulatory guidance as appropriate for safety surveillance. Author safety documents. Lead and set the strategy, in collaboration with the development medical lead of study protocols and informed consents. Proactively engage, coach, and mentor team members and colleagues. Analyze and summarize aggregate safety data and communicate these analysis and interpretation to cross-functional teams and senior management. Implement risk management strategies for assigned products.

Qualifications:
MD / DO required. 2+ years of residency with patient management experience. 8+ years of Pharmacovigilance or Clinical Development experience in the pharmaceutical industry. Ability to present effectively, both internally and externally. Be able to analyze and guide analysis of clinical data.

Please contact Greg Kane at gkane@clarkdavis.com