Oferta de trabajo: Associate Global Medical Director - Global Medical Affairs

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 Associate Global Medical Director will serve as a pivotal leader in advancing the mission of our organization by providing strategic medical expertise, guidance, and vision in the development and execution of our global development portfolio.

This role is dedicated to ensuring the highest standards of scientific integrity, patient safety, regulatory compliance, and collaboration across therapeutic areas. Ultimately, this position aims to support the global health objectives of the organization thought evidence-based medical leadership and a commitment to excellence in all aspects of clinical practice and scientific exchange.

Vision Statement

US East Coast Hub drives innovative strategies to advance our MASH, cardiomyopathy, and advanced technology portfolios for the benefit of patients, fostering a collaborative and inclusive culture within our One Development organization.

Relationship

Reports to the Executive Director Global Medical Affairs East Coast Hub.

Will interact with Global & Affiliate Medical Affairs, Medical & Science, Finance, Human Resources, Project Teams, Global Commercial and Access, Boston Global Development leadership team on occasion. May interact with senior leaders/leadership, on occasion.

Essential Functions

• Stakeholder Management

• Ensure effective and impactful cross-functional collaboration with consistent communication across stakeholders (Global Research, Global Development, Market Access, Marketing, Regulatory Affairs, Safety, International Operations, Regions & Affiliates, NN International, Product Supply)

• Grows and develops relationships between Novo Nordisk and Key Opinion Leaders

• Ensures the application and communication of all Novo Nordisk policies, procedures, according to the Novo Nordisk Way, to external stakeholders

• Is the global medical affairs specialist on a specific product/project towards internal/external customers

• Ensures coordination, within team, of content development and related tasks, focusing on global marketing & medical strategies on a product/project level

• Global Medical Affairs strategic planning process: partners with GMA leaders in preparing robust Global Medical Affairs Plans for compounds, assets, and future R&D products that reflect prioritized regional and local needs

• Supports manager in recruiting and onboarding new colleagues

• May Act as proxy for Medical Director in higher-level global committees, e.g. Product Labelling Committee, Safety Committee and Core Brand team

• KOL Engagement:

• Develop, expand, grow, and maintain strong relationships with Global Key Opinion Leaders

• Provide input, develop and execute on global Health Care Professional strategy

• Plan, conduct and execute global meetings plus support speakers in preparation for presentation of NN data at conferences and symposia

• Design and contribute to and execute on Health Care Professional strategy

• Drives and provides relevant input to Key Opinion Leader database

• Proactively plan and engage in the scientific dialogue with global Key Opinion Leaders and HCP

• Gather and analyze medical and scientific feedback & insights from global Key Opinion Leader interactions in advisory boards and strategic discussions at meetings and conferences

• Clinical Activities:

• Manages and drives the development, refinement, and execution of global scientific communication strategy, including scientific communication platforms, global publication plan, and the integrated evidence generation plan

• For Phase II-IIIa, establishes and provides market-oriented medical input to trial design, protocol development, and investigator selection in NN clinical trials

• For Phase IIIb and IV, drives trial design protocol development according to market oriented medical input and investigator selection in NN clinical trials

• Drive additional clinical activities beyond phase 3a (phase 3b workshops, Investigator Spon- sored Studies)

• Evaluation and decision of clinical trial proposals from Regions & Affiliates related to

• Non-Interventional Studies and Health Economics/Outcome Research

• Provide medical input to regulatory documents for product/project (Core Company Data Sheet, Summary of Product Characteristics, new labelling, and labelling change requests from affiliates)

• Plan and execute investigator, results meetings, Global Expert Panel KOL’s and meetings, Scientific Expert Committee meetings

• Communication:

• Transforms the clinical trial data into scientific and commercial communication

• Manages the development, refinement and execution of global scientific communication plat- forms with Patients, Primary and Specialty Health Care Professionals, Key Opinion Leaders, Advisory Boards and Consultative services, Scientific Experts

• Leads on key trial communication strategy

• Ensure organizational readiness with robust communication plans on medical and scientific communication strategies

• Drives scientific communication strategy around our products in outcome studies

• Develops a broad range of medical guidance documents while adapting to needed digital solutions (e.g. e-learnings)

• Ensures alignment of relevant cross-functional medical guidance activities/platforms on specific product/project

• Develop, drive and execute on scientific communication during high quality global meetings (e.g. scientific expert meetings, symposia etc.)

• Project Management:

• Cross-functional collaboration – Global Research, Global Development, Strategy Access Marketing, Medical Affairs Regulatory Safety, International Operations, NN International

• Ensures Medical/scientific support and guidance to Public Affairs and/or Market Access in negotiations with payers/policy makers for specific product/project

• Ensures optimal project and vendor management in the execution of GMA strategies and tac- tics, develop sourcing strategies and effective partnerships with vendors/agencies

• Follow all safety & environmental requirements in the performance of duties

• Other accountabilities as assigned

  Physical Requirements

  Ability to travel occasionally – both internationally and domestically in the U.S. Approximately 20% travel per year to congresses, scientific Novo Nordisk events and affiliate meetings. Hybrid position, can be based either at our Plainsboro NJ or Lexington, MA sites.

  Qualifications

• MD/DO/PharmD with 3+ years or PhD/DNP with 5+ years of substantial clinical and/or research expertise in relevant area (e.g., Endocrinology, Cardiology, General Practice, Internal Medicine, or specialty medicine) required

• Additional education and experience in business administration / marketing is preferred

• Based in the USA, we have a global responsibility covering all or most Novo Nordisk affiliates

• At least 3+ years of clinical and/or pharmaceutical industry experience required

• Experience in a medical, clinical, or scientific environment is required

• In depth knowledge of study methodology, data analysis techniques, and critical review of publications required

• Strong presentation skills, with experience in presenting data at congresses, preferred

• Budget and vendor management experience preferred

• Experience managing publication agencies and/or medical affairs vendors (e.g., advisory board) preferred

• Medical Affairs experience preferred

• Strong communication and organizational skills required

• Ability to drive projects forward to completion while maintaining a focus on the long-term strategy required

• Proven experience in driving results in a highly complex and rapidly changing environment required

• Global mindset with proven ability to partner cross culturally and regionally is preferred

• The job requires skillful stakeholder management, especially with affiliates and the scientific community

  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.