PharmD Program Associate - Safety Sciences

Safety Sciences – Associate will gain working knowledge of pharmacovigilance (PV) disciplines to continuously assess benefit-risk of products across the product life cycle (early clinical development through market authorization and post-marketing), with a focus on signal detection and management. Build foundational knowledge in case processing operations and understand PV business support functions enabling a global pharmacovigilance organization; interface cross-functionally on tasks/projects.

Responsibilities:
- Draft documents integral to clinical sites and regulatory submissions
- Analyze data from clinical studies for interactions with ethics committees, senior management, regulatory authorities, and others
- Manage third-party vendors and maintain timelines of key results
- Develop regulatory strategies for clinical development programs
- Analyze safety data to characterize product safety profiles throughout development
- Work with program mentors to improve skills to reach professional goals
- Travel to clinical sites and/or meetings with health authorities (as opportunities)

Required/Qualifications:
- PharmD from an accredited (ACPE) College of Pharmacy; PhD in a life science area may also be considered
- PharmD and/or PhD completed by Summer 2027
- Prior internship/rotational experience in Pharmaceutical/Biotech (plus)
- Exposure/familiarity evaluating clinical trials, scientific literature, and data
- Eligible to work in the U.S. on a permanent basis

Application:
- Submit resume and cover letter specifying the track of interest; rank tracks if multiple.
- Applications accepted: August 24, 2026 – September 11, 2026.