The Regulatory Affairs Intern will support the Regulatory Affairs team in preparing documentation, tracking submissions, and assisting with project coordination. This internship offers exposure to regulatory processes in the pharmaceutical industry and provides hands-on experience in a cross-functional environment.
The full-time internship will take place June - August 2026.
Essential duties and responsibilities include the following. Other duties may be assigned.
Regulatory Documentation Support
Assist in organizing and formatting regulatory submission documents (e.g., IND, CTA, briefing packages, nonclinical reports)
Help maintain submission trackers and document repositories
Review documents for consistency and completeness under supervision
Project Coordination
Support the creation and updating of project timelines and task lists
Attend team meetings and take notes on action items and follow-ups
Help prepare meeting agendas and distribute materials
Cross-functional Communication
Coordinate with internal teams to gather required documentation
Draft internal communications and summaries for regulatory updates
Shadow cross-functional meetings to understand regulatory integration
Research and Compliance
Conduct literature reviews and regulatory intelligence gathering
Assist in compiling summaries of relevant FDA/EMA guidance documents
Help monitor changes in regulatory requirements and flag updates to the team
Currently pursuing a Bachelor's degree in Life Sciences, Pharmacy, Public Health, or related field
Strong interest in regulatory affairs and drug development
Excellent organizational and communication skills
All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment. Please note that immigration or visa sponsorship is not available for this position.
Familiarity with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and Adobe Acrobat
Experience with project management tools (e.g., Smartsheet, MS Project) is a plus
Prior internship or coursework related to clinical trials or regulatory science
Detail-oriented and able to manage multiple tasks
Strong written and verbal communication skills
Professional, proactive, and eager to learn
Ability to work collaboratively in a dynamic, cross-functional environment
This is a temporary, time-bound position intended for the duration of the internship or co-op program. Employment in this role does not imply or guarantee ongoing or permanent employment with BMS.
The starting hourly compensation for this assignment is within the range of $20.00 to $42.00/hr. Please note that the final individual compensation and any applicable benefits will be determined by your employer of record (and not BMS). Factors influencing this decision may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location of the job. Compensation details are subject to change.
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