2026 U.S Summer Internship Program: Marketed Products Development (MPD) CPASS and Clinical Science Intern

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Job Description

This is a joint internship with The Center for Post-Approval Safety Studies (CPASS) and Clinical Science within the Marketed Products Development (MPD) function. CPASS is responsible for the design, execution, and oversight of global post-marketing safety studies including Post-Authorization Safety Studies (PASS) and Post Marketing Surveillance (PMS) Studies. CPASS has broad reach and partners with functions across R&D, Safety, Regulatory, and Medical Affairs to generate real-world evidence that supports product safety and regulatory commitments. The MPD Clinical Science function leads post-marketing clinical strategy and execution, including interventional trials for pediatric development, label enhancements, new formulations or doses, and geographic expansion. The team conducts post-marketing requirement and commitment studies to ensure continued availability of safe and effective medicines, working in close collaboration with a broad range of functions across Takeda.

MPD sits within Global Medical (GM), which is part of the Global Portfolio Division (GPD).

How You Will Contribute:
As an MPD CPASS and Clinical Science Intern, you will have the opportunity to:

• Support the oversight of post-marketing safety study commitments.

• Support the development and maintenance of Standard Operating Procedures (SOPs) and process documents related to post-marketing safety studies.

• Contribute to cross-functional meetings by preparing slide decks, summaries, and action trackers.

• Support the review of study protocols and study-related documentation for quality and compliance.

• Assist in ad-hoc projects to streamline operational processes and improve team efficiency.

• Under the guidance of the Clinical Science Lead, you will:

  • Attend team and cross-functional meetings to gain exposure to Clinical Science, MPD programs/products and other functions (e.g. clinical operations, biostatistics, regulatory affairs, clinical pharmacology, etc.).

  • Support monitoring of ongoing studies and study completion activities (e.g., data review, results and report review).

  • Contribute to literature reviews, if assigned, and other project work.
     

Internship Development Opportunities:

• Gain exposure to the context and execution of post-marketing safety studies within a global pharmaceutical company.

• Gain exposure to planning and execution of interventional clinical studies and assessment of clinical efficacy.

• Develop skills in evidence generation, regulatory compliance, and cross-functional collaboration.

• Build professional networks across CPASS, Clinical Science, MPD, and R&D.

• Enhance critical thinking and communication skills through active contribution to real-world projects.
   

Job Requirements:

• This position will be Hybrid (8+ days per month in office) out of the Cambridge, MA location.

• Must be pursuing a Masters or Doctoral degree in Public Health, Epidemiology, Pharmaceutical Sciences, Life Sciences, Biostatistics, Health Policy, or a related field.

• Strong written and verbal communication skills.

• Ability to work independently and collaboratively in a fast-paced, matrixed environment.

• Strong analytical skills, attention to detail, and proficiency with Microsoft Office Suite (Excel, PowerPoint, Word).

Internship Eligibility 

• 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 depending on the two start dates (May 26th-August 14th or June 15th- August 21st)  

• The intern must be able to commit to one of these time frames  

• Able to work full time 40 hours a week during internship dates  

• Takeda does not provide a housing stipend or relocation support for the U.S Summer Internship Program 

 Program Highlights: