Regulatory Affairs Fellow, CVRM – Hybrid (Kendall)

Northeastern University; Boston (MA); Hybrid; USD 60,000 - 85,000; Full time

Job summary

Northeastern University, in Boston, in partnership with AstraZeneca, offers a two-year CVRM Regulatory Affairs fellowship as part of the Pharmaceutical Industry Fellowship Program. The position is based at Kendall Square with hybrid work, focusing on regulatory strategy and lifecycle management for small- and large-molecule medicines.

As a Regulatory Affairs Fellow you will contribute to global regulatory strategies, collaborate across disciplines, and build leadership skills while pursuing

Qualifications

• Doctor of Pharmacy degree from ACPE-accredited institution.
• Eligible for pharmacist licensure in the State of Massachusetts.
• Excellent oral and written communication and presentation skills.
• Strong time management and leadership abilities.
• Ability to work independently and take initiative on a variety of projects at both the industry site and Northeastern.
• Ability to work as part of a team.
• Strategic-oriented mindset with attention to detail.
• Fluent in the use of AI tools for research and efficiency in the workplace.

Responsibilities

• Contribute to global regulatory strategies across the CVRM portfolio.
• Provide regulatory leadership and strategic input for development programs.
• Collaborate with AstraZeneca and Northeastern teams to advance lifecycle management.
• Support development, registration, and commercialization activities across product pipelines.

Skills

Communication

Time management

Leadership

Independent work

Team collaboration

Strategic thinking

AI tools fluency

Education

Doctor of Pharmacy (ACPE-accredited)

Job description

Northeastern University, in Boston, in partnership with AstraZeneca, offers a two-year CVRM Regulatory Affairs fellowship as part of the Pharmaceutical Industry Fellowship Program. The position is based at Kendall Square with hybrid work, focusing on regulatory strategy and lifecycle management for small- and large-molecule medicines.

As a Regulatory Affairs Fellow you will contribute to global regulatory strategies, collaborate across disciplines, and build leadership skills while pursuing