Principal Medical Writer (Plainsboro, NJ or Lexington, MA)

About the Department

Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple innovative modalities and therapeutic areas. Our East Coast Global Development 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. We recognize that improving human health starts here and that patients rely on us. We’re changing lives for a living. Are you ready to make a difference?

The Position

The Principal Medical Writer is an expert in medical writing and performs work independently with minimal-to-no supervision. The Principal Medical Writer will work closely with cross-functional project teams, including Medical & Science, Clinical Operations, Biometrics, and Regulatory Affairs personnel, to manage preparation of the written deliverables that support the clinical development and regulatory requirements of a clinical program. The Principal Medical Writer will provide high level strategic input into development plans, study designs, and regulatory submissions.

Relationships

The Principal Medical Writer reports to a Director of Medical Writing.

The Principal Medical Writer is expected to develop and maintain a strong network of internal relationships with global and local cross-functional study teams.

The Principal Medical Writer should be seen as a key resource for medical writing expertise and provides active leadership on local and global project teams, as needed.

The Principal Medical Writer will provide mentoring and direction to less-experienced medical writers, as needed.

Essential Functions

• Provides strategic input into documents and plans to support clinical operations and regulatory submissions across a range of development programs and therapeutic areas:
• Uses professional experience to provide advanced input into study designs, analysis plans, and regulatory submissions/ applications
• Analyzes proposed study plans and related documents for their ability to deliver the information required by the target audience
• Collaborates with others to develop key messages for complex clinical/regulatory documents

Physical Requirements

Less than 10% overnight travel. May include travel outside the US.

Qualifications

• Education Level:
• Minimum of BS/BA, preferably in a health-related or scientific discipline

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.