Hybrid Regulatory Affairs Fellow, CVRM

NU USA Northeastern University

Boston (MA)

Hybrid

USD 60,000 - 85,000

Full time

14 days+

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Job summary

Northeastern University is offering a two-year CVRM Regulatory Affairs fellowship in collaboration with AstraZeneca, based in Cambridge, MA with a hybrid work arrangement in Kendall Square.

The role focuses on global regulatory strategies for drug development, with opportunities to lead and influence regulatory decisions as experience grows. A Doctor of Pharmacy degree and MA licensure eligibility are required.

Qualifications

  • Doctor of Pharmacy degree from an 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

  • Join a Regulatory Affairs team to drive regulatory strategy and support development, commercialization and lifecycle management of products.
  • Engage with Health Authorities to inform development programs and ensure compliance.
  • Provide strategic and operational regulatory support as experience increases, potentially serving as regional regulatory lead.
  • Contribute to crafting and implementing clinical strategies and influencing stakeholders to improve outcomes.

Skills

Communication
Time management
Leadership
Initiative
Teamwork
Strategic mindset
AI tools

Education

Doctor of Pharmacy degree

Tools

AI tools

Job description

Northeastern University is offering a two-year CVRM Regulatory Affairs fellowship in collaboration with AstraZeneca, based in Cambridge, MA with a hybrid work arrangement in Kendall Square.

The role focuses on global regulatory strategies for drug development, with opportunities to lead and influence regulatory decisions as experience grows. A Doctor of Pharmacy degree and MA licensure eligibility are required.

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