Dir GMA Oncology
Company: Daiichi Sankyo
Location: Basking Ridge
Posted on: January 31, 2026
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Job Description:
Job Description Job Title: Dir GMA Oncology Job Requisition ID:
743 Posting Start Date: 1/15/26 At Daiichi Sankyo, we are united by
a single purpose, to improve lives around the world through
innovative medicines. With a legacy of innovation since 1899, a
presence in more than 30 countries, and more than 19,000 employees,
we are advancing breakthrough therapies in oncology, cardiovascular
disease, rare diseases, and immune disorders. Guided by our 2030
vision to "be an innovative global healthcare company contributing
to the sustainable development of society", we are shaping a
healthier, more hopeful future for patients, their families, and
society. Job Summary The Director Global Medical Affairs Oncology
(GMA), ADC, under the direction of the Senior Director, GMA
Oncology ADC (Global Medical Affairs team lead for compound), is
responsible for assisting with defining compound/program medical
strategies and for leading select medical affairs projects within a
specific compound or indication. Responsibilities Leads the
development of the Global Medical Affairs strategy and execution of
the Global Medical Affairs plan for select indications/projects
related to evidence generation, medical information and internal
education, publications, scientific exchange and external data
communication, and stakeholder scientific engagement. Responsible
for managing budgets and resources for the assigned GMA plan
activities, in collaboration with Sr Director. Leads medical
readiness activities for market launches and life cycle management
for select indications/projects. Gains strategic and planning
alignment across regions and functions and supports review of Local
Country/Regional Medical Affairs activities when applicable.
Provide medical support/input into commercial and market access
discussions for select indications. Serve as medical lead for
select company-sponsored GMA evidence generating studies/projects.
Manages all medical aspects such as study document development and
drives execution for assigned projects in collaboration with GMA
Clinical Operations and other cross-functional and regional
stakeholders. Provides support in review of investigator-initiated
studies (IIS) and may serve as deputy compound lead in Global IIS
Review Committee meetings. Leads external medical education and
other scientific exchange activities in alignment with the Senior
Director, such as scientific symposium and medical congresses,
within legal and compliance regulations. Collaborates across
functions to support GMA MI&E activities in order to achieve
approval of key scientific communications resources such as medical
information response documents, (non-) promotional materials,
educational slide deck and other internal training resources,
within legal and compliance regulations. Provide training or
communication of emerging data (internal or competitive), such as
congress updates and development program highlights. Provides
medical leadership in interactions with key external stakeholders
and lead Scientific Engagement activities such as planning advisory
boards, managing individual stakeholder interactions and peer to
peer discussions, congress engagement activities, and collation of
insights for select indications related to the compound. Provides
support in the review of GMA Publications (abstracts,
presentations, and manuscripts) and may serve as deputy compound
lead on the Publication Planning Subteam (PPS). Qualifications
Education Qualifications PharmD An advanced doctorate degree
(PharmD, PhD, MD, DO or equivalent) in medical/ scientific area is
required. Experience in oncology therapeutic area is required
required or PhD An advanced doctorate degree (PharmD, PhD, MD, DO
or equivalent) in medical/ scientific area is required. Experience
in oncology therapeutic area is required required or MD An advanced
doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical/
scientific area is required. Experience in oncology therapeutic
area is required required or DO An advanced doctorate degree
(PharmD, PhD, MD, DO or equivalent) in medical/ scientific area is
required. Experience in oncology therapeutic area is required
required Experience Qualifications 10 or more years of professional
pharmaceutical industry experience with medical affairs or other
relevant experience 4 or More Years experience in pharma at local,
regional and/or Global level. Excellent knowledge of current
clinical practice in Oncology / Hematology / Endocrinology or other
relevant disease area strongly preferred. Must have knowledge in
and understanding of medical activities (including scientific
communications, medical information, MSLs, and HEOR), relating to
the commercialization of oncology products Travel Requirements
Ability to travel up to 20% of the time. Standard office based
physical demands, travel as required. Daiichi Sankyo, Inc. is an
equal opportunity/affirmative action employer. Qualified applicants
will receive consideration for employment without regard to sex,
gender identity, sexual orientation, race, color, religion,
national origin, disability, protected veteran status, age, or any
other characteristic protected by law. Salary Range: USD$206,800.00
- USD$310,200.00 Download Our Benefits Summary PDF
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Keywords: Daiichi Sankyo, Levittown , Dir GMA Oncology, Science, Research & Development , Basking Ridge, New York