Insulet Corporation

  • European Medical Lead

    Job Locations UK-London | UK-London
    Posted Date 3 months ago(5/23/2019 11:46 AM)
    Category
    Regulatory Affairs / Clinical Affairs
  • Position Summary

    • This position offers the opportunity to build the Medical Affairs function and team from the ground up at a rapidly growing, innovative global diabetes technology company.
    • This role is responsible for developing and executing a strategy for key thought/opinion leader (KOL) engagement. This includes establishing, fostering, cultivating and maintaining relationships with KOLs as a conduit for accurate and updated clinical, scientific and medical information between KOLs and the company.
    • The individual in this role will work closely with Insulet’s cross-functional teams to ensure the information, education, and research needs of HCPs are met and to ensure scientific and technical training needs of commercial and advocacy organizations are identified and met.
    • The individual in this role will have an in-depth understanding of the diabetes disease state, the current/future treatment landscape, and ongoing clinical trials/research.  

    Responsibilities

    • Lead clinical and scientific exchange with KOLs, HCPs and practices regarding the companies marketed and pipeline products and diabetes care technology
    • Establish and maintain credible peer-to-peer scientific relationships with national/regional KOLs and prescribers
    • Facilitate KOL involvement in national, regional, and local educational forums including advisory boards, congress symposia, and sponsored educational and promotional programs
    • Create and maintain a library of slides/decks to support scientific exchange and conference presentations
    • Assist in the development of education and training materials for internal teams to increase understanding of the diabetes therapeutic landscape and competitors
    • Lead scientific and medical congresses planning and attend sessions to capture information relevant to the organization’s scientific platforms and report this information to senior leadership and internal stakeholders
    • Attend scientific and medical congresses to capture information relevant to the organization’s scientific platforms and report this information to senior leadership and internal stakeholders
    • Participate in Legal Medical Regulatory (LMR) meetings to provide medical review of promotional material
    • Maintain a thorough and detailed working knowledge of the organization and its products, current scientific research and publications
    • Support in-person responses to requests for medical information
    • Performs other duties as required

    Education and Experience

    Minimum Requirements:

    • PharmD, PhD in a life science or MD
    • 10 years+ relevant MSL experience in the diabetes pharmaceutical or medical industry
    • Expert knowledge of the medical device industry, including relevant laws (TBD EU), regulations (TBD EU), and ethical standards (TBD EU) which apply to interactions with HCPs, payers, and industry representatives
    • In-depth understanding of the diabetes disease state, the current/future treatment landscape, and ongoing clinical trials/research
    • Understanding of the medical practice and clinical decision making regarding patient care for diabetes
    • Demonstrated ability to integrate and work in a challenging cross-functional environment
    • Excellent written and effective verbal communication skills

     Physical Requirements (if applicable):        

    • This role will involve frequent travel, 25 to 50% through Europe
    • Corporate office based in London

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