Summer Intern - Clinical Development
About The Position
Insmed is seeking a Summer Intern to support its Clinical Development Team in planning, execution, and oversight of clinical development activities across studies. The 2027 Summer Internship Program is a paid, full-time (40 hours per week), 12-week program offering hands-on experience, meaningful team projects, and the opportunity to learn from experienced professionals. Rotational assignments within the function may be available, and the intern will receive goals and objectives that support the company’s strategic business plan. The intern will gain exposure to clinical data review, safety surveillance, benefit-risk assessment, and collaboration across the clinical trial lifecycle. This is a fully remote role that may be performed from anywhere while remaining connected to the Insmed team and community. Occasional travel for team meetings or events may be expected.
Requirements
- Currently enrolled as a student working toward a PharmD, master’s degree, or PhD.
- Strong interest in pharmaceutical or biotechnology clinical development.
- Demonstrated ability to work with data and identify patterns or inconsistencies.
- Strong organizational skills and a high level of attention to detail.
- Excellent written and verbal communication skills.
- Ability to manage multiple assignments and meet established deadlines.
- Ability to work collaboratively in a cross-functional team environment.
Nice To Haves
- Coursework in clinical research or drug development.
- Previous exposure to clinical trials, clinical research, healthcare, or pharmaceutical or biotechnology environments.
- Familiarity with clinical trial terminology and concepts.
- Experience with data visualization or data analysis tools.
Responsibilities
- Support the Clinical Development team in planning, executing, and overseeing clinical development activities across studies.
- Assist with routine review of patient-level and aggregate clinical trial data, including demographics, medical history, laboratory results, vital signs, and adverse events and serious adverse events; identify trends, inconsistencies, or signals for escalation.
- Collaborate with Clinical Operations and Data Management to resolve data issues and periodically track enrollment, discontinuations, protocol deviations, and safety events.
- Compile data and prepare agendas, summaries, and presentation materials for monthly internal Medical Monitoring meetings.
- Coordinate cross-functional updates and maintain meeting documentation.
- Prepare post-meeting summaries of decisions and action items and ensure follow-up.
- Collaborate with Clinical Development, Clinical Operations, Data Management, Biostatistics, Pharmacovigilance, Regulatory Affairs, and other stakeholders.
- Gain exposure to the relationship between clinical data review, safety surveillance, and benefit-risk assessment.
- Complete assigned goals and objectives in support of the company’s strategic business plan.
Benefits
- Paid company holidays
- Hands-on learning in real-world projects
- Networking opportunities with leaders and social events with peers
- Mentorship and professional development
- Final presentation celebrating the intern’s 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
