Postdoctoral Research Fellow, Blueprint--Regulatory Affairs

Northeastern University • Boston, MA

414d

About The Position

The Postdoctoral Research Fellow in Regulatory Affairs at Northeastern University, in collaboration with Blueprint Medicines, is a two-year fellowship aimed at advancing the education and training of Pharm.D. graduates in the biopharmaceutical industry. This role provides hands-on regulatory experience within a rapidly growing biotechnology company, focusing on various aspects of regulatory affairs, including clinical trials and regulatory submissions.

Requirements

• Doctor of Pharmacy degree from an ACPE accredited institution, eligible for licensure as a pharmacist in the State of Massachusetts.
• Excellent oral and written communication skills.
• Strong time management and leadership skills.
• Ability to work independently and take initiative on a variety of projects.

Responsibilities

• Manage the development and execution of regulatory submissions for assigned projects.
• Contribute to the development of regulatory strategy for life cycle management of Blueprint Medicines clinical programs.
• Summarize key insights from global drug approvals, applying lessons to Blueprint Medicines clinical programs.
• Collaborate with internal and external partners across drug development and commercialization continuum.
• Develop and deliver presentations as needed to the regulatory team and other internal groups.
• Contribute to activities in support of high-quality regulatory documentation.

Benefits

• Medical insurance
• Vision insurance
• Dental insurance
• Paid time off
• Tuition assistance
• Wellness programs
• Life insurance
• Retirement benefits
• Commuting and transportation assistance

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Educational Services
• Education Level: Ph.D. or professional degree