Global Regulatory Affairs Fellow (2-Year Postdoc)

NU USA Northeastern University

Boston (MA)

On-site

USD 60,000 - 85,000

Full time

14 days+

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Job summary

Alnylam Pharmaceuticals, in partnership with Northeastern University, offers a two-year Regulatory Affairs fellowship based in Cambridge, MA. The program develops expertise in global regulatory strategy, with exposure to diverse regulatory disciplines and cross-functional collaboration across the drug development lifecycle.

The Fellow will work closely with NEU faculty and industry partners, gaining experience in regulatory submissions, strategy development, and project management in a dynamic

Qualifications

  • Doctor of Pharmacy degree from an ACPE-accredited institution.
  • Eligible for pharmacist licensure in the State of Massachusetts.
  • Excellent oral and written communication 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

Responsibilities

  • Support regulatory filings and submissions across US and international programs.
  • Participate in cross-functional meetings to support regulatory strategy and development plans.
  • Conduct guidance and precedent research to support regulatory strategy.
  • Assist in development lifecycle submissions for commercial programs.
  • Prepare U.S. and/or international regulatory submissions as assigned.

Skills

Excellent communication
Time management
Leadership
Independent work
Massachusetts licensure eligibility

Education

Doctor of Pharmacy degree

Job description

Alnylam Pharmaceuticals, in partnership with Northeastern University, offers a two-year Regulatory Affairs fellowship based in Cambridge, MA. The program develops expertise in global regulatory strategy, with exposure to diverse regulatory disciplines and cross-functional collaboration across the drug development lifecycle.

The Fellow will work closely with NEU faculty and industry partners, gaining experience in regulatory submissions, strategy development, and project management in a dynamic

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