Senior Medical Director, Global Medical Affairs Alzheimer’s Disease, Global Medical Evidence Gen
Location: Nutley, New Jersey
Type: Full Time
Required Education: MD
Internal Number: 98912360
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 Senior Medical Director, Global Medical Affairs – Alzheimer’s Disease (AD), Global Medical Evidence Generation in the Neurology Business Group (NBG) provides medical leadership and accountability to the AD portfolio and continued support as a key partner to Clinical Development, Real World Evidence, Discovery and Commercial Operations. The candidate will drive a process to understand barriers and knowledge gaps in the AD therapeutic area, orchestrate development and oversee execution and dissemination of strategic evidence generation through the utilization of the integrated evidence generation plans and evidence generation activities for the AD portfolio. The candidate will work in close collaboration with internal functions and external stakeholders to close data gaps required for adaptation, access and ecosystem readiness for disease modifying treatment (DMT) uptake and new product development.
In close collaboration with the Executive Medical Director, Global Medical Affairs AD Ecosystem and Pipeline, this role is responsible for generating data in close alignment with the relevant internal and external stakeholders and building external coalitions with patient and research organizations to enable adaptation of these data/tools to ensure ecosystem readiness and DMT adaptation to serve patients and health care system (HCS) needs. The Senior Medical Director is a key member of the NBG group responsible for developing and maintaining excellence in global medical affairs activities.
The Senior Medical Director will be responsible for developing, implementing, and managing the coordination of all Alzheimer’s Disease-related programs as they relate to the developing medical affairs function and will act as a liaison with global and regional AD medical affairs leads and will provide guidance and resources to these matrixed teams as necessary.
Work with the Executive Medical Director, Global Medical Affairs to develop, coordinate and control annual medical strategy plans and budgets for the global Alzheimer’s therapeutic area
Strategize direction/content, plan, coordinate and execute broad-based activities supporting the Global Medical Affairs team, including educational programs, advisory boards, symposia and congresses as deemed appropriate
Design, plan, direct, and implement medical evidence generation and Phase IV clinical studies or programs for assigned products, with the goal to support approval, optimize labelling while maximizing access for patients with AD, enabling clinical adoption of a new treatment and optimizing medical practice
Build coalitions with external stakeholders to understand treatment pathway barriers and generate and utilize data that enable a better treatment and care for AD patients.
Provide medical oversight for phase IV protocol development, interpretation of trial results, final study report conclusions, and publications. Provide critical medical input into the lifecycle management strategies in responsible therapeutic areas.
Medical/Scientific subject matter expert: Serve as a medical leader and subject matter expert providing direction for assigned products including (but not limited to) 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.
Strong leadership in her/or his area with soft skills to make sure this responsibility is executed with utmost focus to the culture of Eisai and serving patients, their caregivers, and the health care systems
This position requires a dynamic individual with an MD/DO and significant industry experience
In-depth knowledge of the neuroscience and neurobiology of neurodegeneration/dementia/cognition/supportive care diseases, including Alzheimer disease
10 plus years experience
Strong and determined candidate preferably with experience driving holistic and strategic evidence generation across various data sources and in close collaboration with several internal, global and regional and external key stakeholders.
Experience in driving multiple large projects with external and internal stakeholders and impact on patient outcome and/or HCS benefit
Global/regional or large country experience for several years in medical affairs or similar function
Strong and adaptable leadership mind set, self-starter and stimulated by challenges, inclusive and team player, motivated by outcome for patients, good communication skills and able to align different stakeholders views and create win/win solutions, strategic mindset
Strong interpersonal, team building and communication skills
Excellent analytical and data managing skills
Eisai requires all new hires to be fully vaccinated against COVID-19 and provide valid proof of vaccination as of their start date, to the extent permitted under state law. This requirement is a condition of employment at Eisai, and it applies regardless of whether the position is located at an Eisai site, field based or is fully remote. If you are unable to receive the vaccine due to a medical condition (including pregnancy-related), or because of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.
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: