Summer Intern Development Operations
About The Position
At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we're in. Are you? About the Role: We're looking for a Summer Intern - Development Operations on the Clinical Operations to help us expand what's possible for patients with serious diseases. The Insmed Summer Internship Program is designed to give you more than just a glimpse into the pharmaceutical industry—it's a chance to make a real impact. Over the course of the summer, you'll gain hands-on experience, contribute to meaningful team projects, and learn directly from skilled professionals who are invested in your growth. The Insmed Summer Internship Program gives students an opportunity to gain hands-on experience in a corporate environment in the pharmaceutical industry, receive mentoring from highly skilled professionals, and work on dynamic team projects. Our 2026 Summer Intern program is a full-time (40 hours per week), paid internship. The internship may present opportunities for rotational assignments within the function, and the intern will be assigned goals and objectives that will support the strategic business plan of the company.
Requirements
- You are a current student working on a Bachelor's, Master's, or advanced level degree in Biology, Chemistry, Pharmacology, Nursing, or Accounting.
- Interested in pursuing a career in the pharmaceutical industry
- High level understanding of what clinical trials are and their purpose
- Must have excellent communication skills (verbal and written).
- Highly organized with a strong attention to detail, clarity, accuracy, and conciseness.
- Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).
Responsibilities
- Look across the Development Operations (Dev Ops) groups and recommend innovative ways to leverage common technology to work smarter as a group e.g., utilization of Teams, SharePoint Sites
- Rotate between the four Dev Ops groups: Clinical Trial Operations, Clinical Business Operations, Clinical Program Optimization and Innovation, and Medical Writing and Trial Transparency & Disclosure. The responsibilities may change based on the group they are supporting at a given time
- Shadow individuals in various roles within Dev Ops (e.g., Clinical Trial Manager, Clinical Trial Assistant, Trial Master File Specialist, Clinical Finance Manager, Medical Writer, Trial Transparency and Disclosure Manager, Vendor Alliance Manager, Clinical Process Manager)
- Support of special projects and work group initiatives with a goal to enhance Dev Ops ability to conduct efficient, high-quality clinical trials
- Attend Clinical Study Team and Dev Ops meetings to learn more about the Drug Development process and how cross-functional teams work
- Review trial related documents, spreadsheets, and systems to assess the accuracy and completeness of information e.g., clinical site generated documents, Trial Master Files, financial spreadsheets, protocols
Benefits
- Paid company holidays
- Hands-on learning in real-world projects
- Networking opportunities with leaders and social events with your peers
- Mentorship and professional development
- A final presentation to celebrate your contributions
- Access to office amenities for those who are not remote
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Number of Employees
1,001-5,000 employees
