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Internship - Regulatory Affairs

Employer
Novo Nordisk
Location
Lexington, MA
Start date
Feb 22, 2024

View more

Discipline
Regulatory, Regulatory Affairs
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Genetown, Best Places to Work

Job Details

About the Department

The Lexington Site is home to a growing Development organization, part of Novo Nordisk following its acquisition of Dicerna Pharmaceuticals, Inc. in December 2021. The Lexington Development team is responsible for leading the clinical advancement of Dicerna’s research pipeline of GalXC™ and GalXC-Plus™ RNAi investigational therapies and select candidates from the broader Novo Nordisk portfolio, targeting both rare and prevalent diseases. The Lexington Development team’s rich heritage of collaboration, calculated risk-taking and agility complemented by the scale and resources of the global Development organization, define a unique clinical development team that maintains its agility to efficiently advance clinical candidates through development. Located in one of the most vibrant biotechnology innovation hubs in the world, and part of the growing biotech ecosystem in Lexington, Massachusetts, the Lexington Site will offer you the opportunity to collaborate with extraordinary talent and to continuously develop, while working toward our collective mission to improve patient lives. Together, we are driving change. Are you ready to make a difference? 

 

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 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 3rd, 2024.

Program End: August 9th, 2024.

 

Scope of Position

The Regulatory Affairs intern may be responsible for researching and analyzing regulatory requirements and guidelines related to the products or services of the company. This can include reviewing regulations from different countries or regions, as well as staying up-to-date on any changes or updates in these regulations. The intern may also be responsible for helping with preparation of regulatory submissions, including compiling and organizing documentation, filling out forms, and ensuring that all regulatory requirements are met. Another area the intern may be responsible is for writing and reviewing regulatory documents such as labeling, instructions for use, and regulatory reports. This may involve working closely with other teams such as marketing, quality assurance, and clinical research. The intern may be responsible for supporting the regulatory compliance efforts of the company. This can include assisting with internal audits, monitoring regulatory changes, and ensuring that the company is following all applicable regulations. Intern may be asked to participate in team meetings and projects related to regulatory affairs. This will provide valuable insight into how regulatory affairs into the overall business strategy of the company

 

Physical Requirements

  • 0% overnight travel required.
  •  

    Qualifications

  • Must be a current student enrolled or recently graduated (graduation date no earlier than April 2024) at/from an accredited college or university pursuing at least a bachelor’s degree.
  • A completed or in progress Masters degree in Biology, Biotechnology, Science, Pharmaceutical, 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.

     

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

     

    At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

     

    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.

    Company

    Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

    Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by 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. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.

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    Company info
    Website
    Phone
    617-612-6200
    Location
    75 Hayden Avenue
    Lexington
    MA
    02421
    United States

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