Full-Time

Regulatory Fellow

Posted on 5/9/2026

Northeastern University

Northeastern University

Compensation Overview

$76.3k - $107.8k/yr

Boston, MA, USA

Hybrid

Hybrid-Eligible: up to two remote days per week; On-Site option available.

Category
Legal & Compliance (1)
Requirements
  • Successfully completed a Doctoral program in a scientific background within the last two years
  • Understanding of drug development and related concepts, such as clinical trial design, statistics, and clinical pharmacology
  • Ability to assess and understand complex scientific information
  • Strong problem-solving skills
  • Strong written and verbal communication skills to exchange complex information with others in complex situations
  • Ability to work effectively within a team environment
  • Ability to plan, prioritize, and contribute to work and projects in a systematic and efficient manner
  • Ability to start in July at our corporate office in Boston
Responsibilities
  • Contributes to the development and implementation of regulatory strategy for assigned region as a member of the Global Regulatory Affairs functional team
  • Develops proficiency in regional and global regulatory skills
  • Supports global regulatory strategy under guidance of the Global Regulatory Lead
  • Supports regulatory communications with local health authority; under supervision, may support regulatory interactions with the health authority
  • Identifies regulatory requirements for development and approval pathways for assigned region
  • Under supervision, manages the process for preparation, submission, and approval of regulatory applications within assigned region
  • Provides technical regulatory input for key product development or registration documents
  • Works to ensure compliance of regulatory submissions with current regulations and guidance
  • Reviews regulatory intelligence and guidance information to continuously support regulatory strategy in assigned region
  • Informs regulatory affairs senior management on the status of regulatory strategies and tactics, procedures and practices
  • Contributes to the development and implementation of regulatory CMC strategy for assigned region as a member of the Global Regulatory Affairs functional team
  • Develops proficiency in regional and global regulatory skills
  • Supports global regulatory CMC strategy under guidance of the CMC Regulatory Lead
  • Responsible for regulatory communications with local health authority; under supervision, may support regulatory interactions with the health authority
  • Under supervision, manages the process for preparation, submission, and approval of CMC sections of regulatory submissions within assigned region
  • Provides regulatory CMC guidance to cross-functional teams and key stakeholders
  • Works to ensure compliance of regulatory CMC submissions with current regulations and guidance
  • Reviews regulatory intelligence and guidance information to continuously support regulatory CMC strategy in assigned region
  • Informs regulatory affairs senior management on the status of regulatory strategies and tactics, procedures and practices
Northeastern University

Northeastern University

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