Director Global Medical Affairs Oncology
vor 3 Wochen
Datum: 27.04.2024
Passion for Innovation. Compassion for Patients.
Daiichi Sankyo and its 16,000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In Europe, we focus on two areas: In the cardiovascular space, our strong portfolio of medicines reflects our long-standing commitment and shows that we care for every heartbeat; in oncology our goal is to become a global pharma innovator until 2025 by providing novel therapies to patients across the world. Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries. For more information: .
For our headquarters in Munich we are seeking highly qualified candidates to fill the position:
Director Global Medical Affairs Oncology (GMA) (m/f/x) The Position:The Director Global Medical Affairs Oncology (GMA) (m/f/x), 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) an may serve as deputy compound lead on the Publication Planning Subteam (PPS).
Personal Skills and professional experience:An advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical/ scientific area is required. Experience in oncology therapeutic area is required
10 or More Years overall relevant experience would be a plus
4 or More Years experience in pharma at local, regional and/or Global level is preferred
Excellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other relevant disease area
knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products
Demonstrates strong scientific expertise within assigned therapeutic area(s) within the franchise
Effectively manages activities and optimize resources and budget to meet business needs; have excellent project management skills
Build strong internal and external relationships with diverse stakeholders to maximize alignment and organizational effectiveness
Conduct medical/legal review
Operational knowledge and experience in prospective and/or retrospective study design and all stages of study conduct (Start-up, Execution, Analysis, Reporting)
Effectively engage external stakeholders across a broad range of audiences and activities such as evidence generation projects, publications, medical information and education, Advisory Boards, Scientific Exchange)
Provide training to internal customers
Review scientific communications resources and publications
Expertly manage ambiguity and highly complex situations
Have excellent communications skills and ability to convey complex scientific concepts simply and effectively
Internal Project and Budget Accountability
Fluent English (oral and written)
What we offer Working at Daiichi SankyoAt Daiichi Sankyo in Europe, we offer a workplace where your voice is heard. Everything we do, we do with a high level of commitment and a clear focus on patients’ needs. We know that our bold ambition to change patients’ lives for the better can only be achieved through the power of collaboration and the exploration of new approaches. Thus, we encourage our colleagues across Europe to be courageous, to bring their ideas to the table and to embrace opportunities to grow. When you join our European family, you will be a part of a dynamic company where everyone, no matter their role, rolls up their sleeves and gets things done.
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