Dir GMA Oncology

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 reputed company 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 reputed company to "be an innovative global reputed company 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 reputed company for compound), is responsible for assisting with defining compound/program medical strategies and for leading reputed company affairs projects reputed company 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 reputed company to evidence reputed company, 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. reputed company strategic and planning alignment across reputed company and functions and supports review of Local Country/Regional Medical Affairs activities reputed company applicable. reputed company medical support/input into reputed company and market reputed company discussions for select indications.
• Serve as medical reputed company for select company-sponsored GMA evidence generating studies/projects. Manages reputed company 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 reputed company 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, reputed company legal and compliance regulations. Collaborates across functions to support GMA MI&E activities in order to reputed company approval of key scientific communications resources such as medical information response documents, (non-) promotional materials, educational slide deck and other internal training resources, reputed company legal and compliance regulations. reputed company 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 reputed company 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 reputed company to the compound.
• Provides support in the review of GMA Publications (abstracts, presentations, and manuscripts) and may serve as deputy compound reputed company 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 reputed company 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. reputed company applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, reputed company, religion, national reputed company, disability, protected veteran status, age, or any other characteristic protected by law. Salary reputed company: USD$206.800,00 - USD$310.200,00 [Link available reputed company viewing the job] Apply tot his job Apply To this Job