CVRM Regulatory Affairs Postdoctoral Research Fellow

About the role

This two‑year CVRM Regulatory Affairs fellowship, offered in partnership with Northeastern University, provides a unique opportunity to work at AstraZeneca’s new facility in Kendall Square, Cambridge, MA. Fellows will engage in regulatory strategy across the drug‑development lifecycle for cardiovascular, renal and metabolism medicines.

Key responsibilities

• Support global regulatory strategies and contribute to the development, commercialization and lifecycle management of assigned products.
• Provide strategic and operational regulatory support, potentially serving as regional regulatory lead for programs.
• Collaborate with cross‑functional teams and engage with health authorities to inform development programs.

Required profile

• Doctor of Pharmacy (PharmD) degree from an ACPE‑accredited institution.
• Eligible for pharmacist licensure in Massachusetts.
• Excellent oral and written communication, presentation, time‑management and leadership abilities.
• Ability to work independently and as part of a team on industry‑site and university projects.

Required skills

• Fluent use of AI tools for research and workplace efficiency.
• Strong strategic‑oriented mindset with attention to detail.