Regulatory Affairs Intern Job at Bristol Myers Squibb, Indianapolis, IN

  • Bristol Myers Squibb
  • Indianapolis, IN

Job Description

Bristol Myers Squibb is hiring a regulatory affairs intern for a full-time position from June to August 2027 at the Indianapolis site. The intern will support documentation preparation, submission tracking, and project coordination within the regulatory team while gaining exposure to pharmaceutical regulatory processes.

Responsibilities

  • Organize and format regulatory submission documents such as IND, CTA, and briefing packages
  • Maintain submission trackers and document repositories; review documents for consistency
  • Support creation of project timelines, attend team meetings, prepare agendas and materials
  • Conduct literature reviews and regulatory intelligence gathering on FDA/EMA guidance
  • Coordinate with internal teams to gather documentation and draft regulatory update communications

Requirements

  • Currently pursuing Bachelor's degree in Life Sciences, Pharmacy, Public Health, or related field
  • Strong interest in regulatory affairs and drug development
  • Excellent organizational and written communication skills
  • US work authorization; no visa sponsorship available
  • Proficiency with Microsoft Office Suite and Adobe Acrobat (preferred)
  • Detail-oriented with ability to manage multiple tasks simultaneously

Compensation: $24.00 - $45.00 hourly

Job Tags

Hourly pay, Full time, Work at office, Visa sponsorship

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