Ironwood Pharmaceuticals-regulatory Affairs Postdoctoral Research Fellow

Ironwood Pharmaceuticals

Boston, Massachusetts, United States
Base: $59,425.00 - $83,935.00; bonus/equity: not s...
Regulatory submissions for clinical trials
Ind/cta/nda/maa preparation
Global regulatory strategy development
This two-year fellowship prepares PharmD graduates to become individual contributors in Global Regulatory Affairs within the pharmaceutical industry

Job Summary

  • This two-year fellowship prepares PharmD graduates to become individual contributors in Global Regulatory Affairs within the pharmaceutical industry.
  • Fellows will gain practical experience in maintaining INDs, NDAs, and MAAs while collaborating with cross-functional teams including clinical development and quality compliance.
  • The program offers comprehensive training in regulatory strategy, agency interactions, and lifecycle management of therapies for gastrointestinal and rare diseases.

Matching Summary

This two-year fellowship prepares PharmD graduates to become individual contributors in Global Regulatory Affairs within the pharmaceutical industry.

Salary

Base: $59,425.00 - $83,935.00; Bonus/Equity: Not specified; Benefits: Medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement, commuting & transportation

Skills & Requirements

Must-have

  • Regulatory submissions for clinical trials
  • IND/CTA/NDA/MAA preparation
  • Global regulatory strategy development
  • Agency meeting management support
  • Regulatory intelligence monitoring

Nice-to-have

  • Strong interpersonal collaboration skills
  • Vendor oversight experience
  • Analytical and creative problem solving
  • Resilience and proactive feedback seeking
  • Microsoft Office Suite proficiency

Key Requirements

  • Doctor of Pharmacy (PharmD) degree
  • Eligible for pharmacist licensure in Massachusetts
  • ACPE-accredited institution graduation

Work Rights

Not specified

Tailored Resume

Cover Letter