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Role Summary
2026 Summer Internship Program: Global Regulatory Project Management & Strategic Planning (RPM&SP) role supporting GI regulatory operations and milestone planning within Takeda’s GI therapeutic area. Intern will gain hands-on experience in health authority meeting planning, submission timelines, and regulatory scenario planning.
Responsibilities
- Assist in planning and logistics for health authority (HA) meetings, including preparation of timelines, coordination of materials, and tracking key actions.
- Support the development of submission timelines and scenario analyses to evaluate regulatory strategy options.
- Contribute to the preparation of regulatory documentation and project tracking tools.
Qualifications
- This position will be Fully Remote
- Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Regulatory Affairs, Pharmacy, or related field.
- Strong organizational, analytical, and communication skills.
- Interest in regulatory strategy, drug development, and project management.
- Proficiency with Microsoft Office (Excel, PowerPoint, Project/Timeline tools a plus).
- Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship.
- Must be currently enrolled in a degree program graduating December 2026 or later.
- The internship program is 10-12 weeks with two start dates; ability to commit to one timeframe and work full time (40 hours/week).
Skills
- Regulatory operations
- Project management
- Health authority meeting logistics
- Submission planning
- Scenario analysis
- Cross-functional team collaboration
Education
- Currently pursuing Bachelor's or Master's in Life Sciences, Regulatory Affairs, Pharmacy, or related field.
Additional Requirements
- Fully remote work eligibility
- Internship dates: May 26–August 14 or June 15–August 21, 2026
- Able to work full time 40 hours per week during internship dates
- No housing stipend or relocation support provided