Summer Intern - DSPV Operations & Vendor Management

Insmed Inc. • Bridgewater, NJ • 8h ago

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 - DSPV Operations & Vendor Management on the Drug Safety & Pharmacovigilance Team 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.What You'll Do:In this role, you'll have the opportunity to shadow and participate in rotational assignments with functional teams within Drug Safety & Pharmacovigilance to gain a comprehensive understanding of the team's role and responsibilities.You'll also: Learn about other DSPV functional area responsibilities such as Pharmacovigilance (PV) contracts and aggregate reports Engage in Pharmacovigilance (PV) assessment of Product Quality Complaints (PQCs) for Medical Device Reports (MDRs) Collaborate with Information Technology (IT) Team for enhancements to the DSPV mailbox and distribution list processes, including the ServiceNow Request Form and semi-annual Access Update Project Perform regulatory agency E2B submission verifications for Individual Case Safety Report (ICSR) submissions and ensure appropriate documentation Distribute and/or track monthly Regulatory Intelligence (RI) updates to cross-functional colleagues Gain an understanding of the importance of reporting Adverse Events (AEs) and how it impacts the safety profile for Marketing Authorization Holder (MAH) product(s), and its relation to DSPV operational tasks and vendor management Acquire insight into clinical trials and how a new molecular entity may enter the market, and the role that PV holds in this processWho You Are:You are a current student working on a Bachelor's, Master's, or advanced level degree in healthcare related profession or life sciences .You are or you have: Interested in pursuing a career in the pharmaceutical industry Basic level understanding of regulatory guidelines, medical terminology, and Pharmacovigilance processes Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook) Highly organized with a strong attention to quality, detail, clarity, accuracy, and conciseness; in addition to excellent communication skills (verbal and written) Nice to have (but not required): Awareness of EMA Good Pharmacovigilance Practices (GVP) Understanding of adverse events (AE) and/or AE reporting Experience with or knowledge of use of artificial intelligence (AI) Where You'll Work This is a hybrid role based out of our [City, Country] office. You'll work remotely most of the time, with in-per

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