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    Medical Director, US Medical Affairs, Neurology - Nutley, United States - Eisai US

    Eisai US
    Eisai US Nutley, United States

    2 days ago

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    Description
    Medical Director, US Medical Affairs, Neurology - Alzheimer's Disease page is loaded

    Medical Director, US Medical Affairs, Neurology - Alzheimer's Disease

    Apply

    remote type

    Remote

    locations

    United States, Remote

    New Jersey, Nutley

    time type

    Full time

    posted on

    Posted 8 Days Ago

    job requisition id

    R3237


    At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission.

    We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development.

    Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease.

    As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.

    If this is your profile, we want to hear from you.

    The Medical Director, US Medical Affairs provides medical leadership for medical affairs strategy, planning and supportive tactics for assigned therapeutic area.

    This role is responsible for working with key stakeholders to develop and execute the medical affairs plan, including post-marketing research, medical education, research grants, medical advisory boards, and scientific

    communication/publication

    components of overall medical operating plan.

    The Medical Director provides strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department for products in the therapeutic area.

    The Medical Director utilizes expert medical/scientific knowledge in assigned therapeutic area to provide strategic input for the development of product strategies and liaises with external stakeholders to solicit feedback and strengthen Eisai's medical reputation in the disease state community.

    The Medical Director is responsible for approval of medical and scientific content of all relevant

    materials/communications.

    Essential Functions:

    Medical Affairs Strategic Plans:

    Work with key stakeholders, management, and functional area leads to develop strategic and aligned Medical Affairs Plans for the therapeutic area.

    Communicate and represent these plans to upper management/senior leadership within ESI. Continuously update plans and inform stakeholders of progress.

    Phase IV Clinical Studies:
    Direct and design strategies, planning and implementation of Phase IV clinical development programs for assigned products. Provide medical oversight for protocol development, interpretation of trial results, final study report conclusions and publications.
    Serve as study director for trials: Provide critical medical input into the lifecycle management strategies in responsible therapeutic areas


    Medical/Scientific subject matter expert:
    Serve as medical leader and subject matter expert providing direction for assigned products including (but not limited to) CRC, scientific communications, publication planning/review, advisory boards, health outcomes plans, MSL activities, speaker programs,

    investigator-initiated

    research and CME grant reviews or other internal key business processes.

    Responsible for approval of medical and scientific content of Regulatory, Safety, Scientific Affairs, Medical Affairs and Commercial outputs for assigned therapeutic areas.


    External leadership:

    Provides leadership and strategic direction to stakeholders in interactions and communications with external customers, thought leaders, strategic alliances, key organizations, and institutions.

    Maintains external orientation by participating actively in external events and activities. Strengthen Eisai's medical reputation through successful management of medical dimensions of products.


    Requirements:
    Board Certified in therapeutic area and US fellowship training, or MD with 2-4 years' experience in within the pharmaceutical industry including 2 years in-house Medical Affairs role, or PhD or PharmD with 5 years' experience within the pharmaceutical industry, including experience in the therapeutic area and 3 years in an in-house Medical Affairs role; MD preferred
    Clinical research experience, including conducting clinical trials in the Phase IIIb-IV area.
    Expertise in Neurodegenerative Disease; especially Alzheimer's Disease
    Experience reviewing promotional materials from a medical perspective, publications planning, relevant medical society membership and track record of active

    participation/attendance,

    and strong presentation skills.
    Experience working with cross functional medical and commercial teams.
    Therapeutic Area Expertise including standards of care, current medical options for diagnosis and treatment of relevant conditions based upon franchise products
    Understanding Medical Affairs activities
    Understanding of Marketing concepts/strategies
    Knowledge of the pharmaceutical marketplace
    FDA regulations/ICH guidelines regarding conduct of clinical studies in relevant therapeutic area
    Knowledge of regulatory guidance regarding marketing/sales promotional materials
    Strong overall written and verbal communication skills
    Must have requisite skills to function in a complex and dynamic environment, including flexibility and ability to negotiate
    CMJE guidance/general publication practices
    Current ACCME guidelines
    Sound computer skills including Microsoft Word, and PowerPoint
    Familiarity with statistical methodology
    PhRMA Code
    #LI-HC1
    #IND-123

    Eisai Salary Transparency Language:


    The base salary range for the Medical Director, US Medical Affairs, Neurology - Alzheimer's Disease is from :200,900-263,700Under current guidelines, this position is eligible to participate in : Eisai Inc.

    Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.
    Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit

    .
    Certain other benefits may be available for this position, please discuss any questions with your recruiter.

    Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status.

    Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.
    Eisai Inc. participates in E-Verify.

    E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.

    Please click on the following link for more information:

    Right To Work
    E-Verify Participation
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    At Eisai Inc.,

    human health care

    ( hhc ) is our goal. We give our first thoughts to patients and their families, and helping to increase the benefits health care provides. As the U.S. pharmaceutical subsidiary of Tokyo-based Eisai Co., Ltd., we have a passionate commitment to patient care that is the driving force behind our efforts to discover and develop innovative therapies to help address unmet medical needs.

    Eisai is a fully integrated pharmaceutical business that operates in two global business groups: oncology and neurology (dementia-related diseases and neurodegenerative diseases).

    Our U.S.

    headquarters, commercial and clinical development organizations are located in New Jersey; our discovery labs are in Massachusetts and Pennsylvania; and our global demand chain organization resides in Maryland and North Carolina.

    To learn more about Eisai Inc., please visit us at

    and follow us on Twitter

    and LinkedIn .

    All data that is entered should be in the correct case, please refrain from using all caps.
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