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Scientific Director - Obesity East

Employer
Novo Nordisk
Location
Plainsboro, NJ
Start date
Aug 28, 2024
View more categoriesView less categories
Discipline
Clinical, Science/R&D
Required Education
Doctorate/PHD/MD
Position Type
Full time
Hotbed
Pharm Country, Best Places to Work

Job Details

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

The Scientific Director (SD) functions as a subject matter expert to ensure credibility and competency of the medical team and supports strategic projects aligned to the Therapy Area (TA) priorities. The SD works closely with the TA Leadership Team and Medical Director team to identify and execute key projects in a timely fashion. In addition, the SD serves as a key member of the Clinical Trial Strategy Team, provides additional analytic support to the field team, and assists the Program Development and Training function for the TA. SD will engage in direct customer facing activity as needed in support of TA priorities and business needs. 

 

Relationships

This position may report into the Field Director, Medical Affairs (or in smaller TA’s directly into the TA head).  They will coordinate with other TA functions including Medical Directors, Alignment Director, Program Development Director and the Medical Liaison field team both within TA and across other TAs. This position will also coordinate with key functions across CMR (eg NACO), Public and Government Affairs and commercial.  Participate in direct customer engagement activities when needed.

 

Essential Functions

  • Identify and anticipate potential trends, changes to market conditions and areas of opportunity aligned with Therapeutic Area priorities
  • Utilizes subject matter expertise and analytical tools to provide deeper customer knowledge and knowledge of the region to enhance territory management of field teams
  • Lead project teams to manage and support various projects such as digital health, academic training programs, and Professional Associations/Public Affairs/Policy initiatives
  • Work with Program Development and Training to support the overall strategies and plans for scientific resources, communications, and training initiatives for the medical affairs team
  • Serve on Clinical Trial Strategy Team to identify investigators/sites and risks to trial planning and execution, including liaising with NACO to optimize medical support. Support MLs with ISS development, such as providing independent reviewer support when needed
  • Analysis and translation of insights and Competitive Intelligence to inform strategy, develop initiatives and guide plans and priorities
  • Identify, evaluate, and assess new stakeholder groups to determine potential future opportunities
  • Support of other prioritized projects with cross functional teams including marketing, commercial, strategy and innovation, etc
  • Deliver Executive Exchange Education programs aligned with TA needs and priorities, may include Market Access accounts and/or other prioritized stakeholders
  • Assist with advisory boards including Regional, National and/or asynchronous virtual advisory boards and as requested, support presentations of medical data at commercial focus groups
  • Provide feedback and mentoring (aligned with Field and Program Directors) to new hires during on-boarding and provide on-going support, as determined by Field Director
  • Ensure personal compliance with all internal/external SOPs/rules and regulations regarding Novo Nordisk, Inc. (NNI) products, customer interaction, and relationships
  • Support a culture of patient focus, inclusiveness, respect, curiosity, entrepreneurism and be a role model of the Novo Nordisk way
  • Provide ML support for local round tables and other initiatives as requested
  • Additional Commercial Support as Requested:  Delivery of education programs targeted towards HCPs & group practices in collaboration with commercial (i.e., ACLs, RBDs), Support Speakers’ Bureau, including presentations at Speaker Training and Curriculum Development meetings as requested
  •  

    Physical Requirements

    Position is Field Based-Ideal candidate will reside in NJ and cover the following territory (ME, NH, VT, NY, MA, RI, CT, NH, PA, MD, DC, VA). Driver must maintain a valid driver’s license. Must be in good standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. 35 - 50% overnight travel required.

     

    Qualifications

  • Doctorate degree in health sciences from an accredited university (PhD, PharmD, etc) required; MD/DO degree preferred
  • At least 5 years in clinical practice and/or relevant industry experience required    
  • Board Certified/Licensed Clinician in appropriate specialty preferred (Obesity, Metabolic, Cardiometabolic, Endocrinology)         
  • Extensive Disease state knowledge in respective area may be required for Therapeutic Area 
  • Previous experience working in a matrix pharmaceutical organization preferred
  • Strong Presentation Skills required, Prior experience in a teaching/training role preferred           
  • Strong interpersonal, relationship building and communication skills    
  • Demonstrated success of strategic project ideation and execution on local, regional, and national level with measurable outcomes required, global project success desired
  •  

    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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