Manager - Regulatory Affairs - Therapeutic Area

1 month ago

Princeton, New Jersey, United States Novo Nordisk Full time

About the Department

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient-centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a difference?

The Position

Manage and oversee all assigned projects/products/processes. Assist the Director/Associate Director in assuring Novo Nordisk compliance with internal SOPs and Federal and State regulations, including compilation and submission of any required documents to regulatory agencies. Supervise designated personnel.

Relationships

Report to the Director/Associate Director/Lead Regulatory Scientist/Sr. Manager Regulatory Affairs. Develop and maintain positive rapport and working relationships with other personnel in Regulatory Affairs, CMR, and other local and headquarter departments to accomplish company goals. External relationships may include interaction with FDA personnel regarding assigned projects and roles.

Essential Functions

Compile and submit responses to FDA communications. MANAGER, THERAPEUTIC AREA: Compile, submit and maintain applications (IND, NDA, Biologics, Devices) to government agencies in support of research and marketed productsCreate and maintain product/project database to record history of questions asked / responses received during FDA meetingsLiaison between NNI and NNAS departments for preparation of documentation necessary for submission of applicationsMaintain meeting documentation templates and ensure they are current with FDA guidance and Novo Nordisk standardsMaintain up-to-date knowledge of laws, regulations and policies enforced by the Federal and State governments as they relate to pharmaceuticals and devicesMaintain up-to-date knowledge of the data, information, and formats required for inclusion in these applicationsManages simple development projects or portions of projectsMay act as FDA liaison for routine contacts and handles finalization of routine correspondenceMay act as GRT memberOversight of annual reportsParticipate in project team meetings as assignedReview data from contributing departments (including NNAS) and provide comments to assure accurate and complete documents for inclusion in these applicationsReview of regulatory strategy documents; e.g., provides supervisor with input on regulatory strategy documentsSupervise, review and approval of labeling for marketed productsTrack applications through FDA reviewing divisionsWork with project associate on compilation of information and supportive documentation for FDA briefing packagesWork with project leader and team to draft FDA meeting requests and supporting briefing packages for FDA meetings (pre-IND, EOP 2, pre-NDA, pre-BLA) for review by Project LeadersWrite Regulatory documents translating team strategy into regulatory overview documents such as cover letters, pre-meeting package, and other US specific regulatory positioning documents to assist Project Leaders in support of business needs Physical Requirements 0-10% overnight travel required. QualificationsA bachelor's degree required; Life Science and advanced degree preferredA minimum of 4 years of progressively responsible related experience; including hands on related pharmaceutical or medical device/pharmaceutical combination product experience and actual regulatory experienceAdvanced knowledge of pertinent FDA regulationsDetail & deadline oriented; well organizedExcellent verbal & written communication skillsExperience leading projects in specific regulatory area preferredGood interpersonal skills; ability to interact with staff on all levelsKnowledge of diabetes and diabetes management beneficialPrevious supervisory/management experience advantageousWorks independently with minimal supervisionPrevious hands-on experience with compilation and filing of INDs/ NDAs/ Amendments/ Supplements 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 This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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