Plainsboro, NJ, US
9 hours ago
Internship - US R&D Clinical Operations

About the Department

Our Research & Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Plainsboro reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.

 

The Program

At Novo Nordisk, interns will have the opportunity to work closely with experienced industry professionals and gain valuable, hands-on, full-time work experience. For ten working weeks, interns will be immersed in the environment of a global pharmaceutical company and contribute to the line of business by providing sustainable and meaningful project work. Our internship program also includes instructor led trainings, a leadership engagement series, and a guided mentorship program to offer professional and personal development.

 

Program Start: June 1st, 2026

Program End: August 14th, 2026

 

Scope of Position

The intern will support the day-to-day operational activities of the different clinical trials within the Global Clinical Operations team. This position is designed to provide hands-on exposure to the processes and responsibilities involved in managing a global clinical study. Under close supervision, the intern will collaborate with the Clinical Project Lead (CPL) and gain experience in tasks typically performed by Global Trial Managers (GTMs) and Clinical Trial Administrators (CTAs). The intern will assist in coordinating trial-related documentation and tracking activities to ensure compliance with study timelines and quality standards. Responsibilities will include supporting the maintenance of trial management systems, preparing meeting materials, and contributing to the organization of investigator and vendor communications. The intern will also help monitor study progress by reviewing operational metrics and assisting with follow-up actions as directed by the CPL. Additional tasks may involve supporting regulatory and ethics submissions, managing essential documents, and contributing to the preparation of status reports for internal stakeholders. This internship offers an opportunity to learn about cross-functional collaboration in a global setting, understand the complexities of clinical trial execution, and develop foundational skills in project management and clinical operations. The intern will work in a structured environment with guidance and mentorship to ensure a meaningful and educational experience.

 

Physical Requirements

0% overnight travel required.

 

Qualifications

Must be a current student enrolled at an accredited college or university pursuing at least a bachelor’s degree An in progress undergraduate degree in Biology, Biochemistry, Chemistry, Research, or a related discipline preferred Strong academic record with a preferred cumulative GPA of 3.0 or higher Conscientious self-starter with good organizational skills, project management skills and attention to detail Ability to balance multiple projects and priorities, must be able to multi-task Strong interpersonal communication and ability to collaborate with teams; must effectively operate independently, across functional lines, and with internal customers Demonstrated personal initiative, self-motivation, flexibility, adaptability and willingness to learn Proficient in Microsoft Office Tools including Word, Excel, PowerPoint, etc.

 

At this time, Novo Nordisk is not currently hiring individuals for this position who now or in the future would require sponsorship for employment visa status.

 

The base compensation range for this position is $52,000 to $89,000 on an hourly basis. Due to the temporary nature of this program, this position is not eligible to participate in any of the Company's benefit plans and will not be entitled to any paid time off unless otherwise required by applicable law.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

 

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

 

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

 

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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