Medical Management Oncology Europe Solid Tumors/Sarcoma
Medical Management Oncology Europe Solid Tumors/Sarcoma
Daiichi Sankyo Europe
Munich, Germany
The Position:
The Medical Management Oncology Europe Solid Tumors/Sarcoma will provide strategic execution of the European scientific and medical affairs plan to ensure a success pre-launch and post launch activities for Daiichi Sankyo oncology products. He/she will be the regional oncology sarcoma area expert for internal and external stakeholders.
Key responsibilities:
- Develop and ensure the appropriate implementation of the scientific and medical affairs strategy for Pexidartinib in close collaboration with key stakeholders (R&D, Commercial, KAMs, MSLs, etc.);
- Maintain an active network of key opinion leaders and community oncologists with specific focus on sarcoma;
- Provide strategic input to the oncology planning and execution of brand plans at global and regional level;
- Work closely with and influencing clinical development on all aspects, including study design, initiation, and monitoring of clinical studies, phase II-phase IV;
- Interacting with experts at medical meetings, advisory boards, and outreach meetings to represent Daiichi Sankyo and strengthen its reputation in oncology;
- Maintaining external orientation by participating actively in external Oncology events and activities;
- Responsible for timely execution of the European medical affairs plan within budget;
- Acts as the medical expert and leader in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, R&D, global medical affairs);
- Drive the medical affairs activities and generation of key data to support overall product life cycle management and business strategy;
- Be the primary contact for scientific expertise for sarcoma within the medical affairs group for affiliates, global teams, and external experts/customers.
Professional experience and personal skills:
- Medical Doctor (M.D.) degree with relevant therapeutic specialty in oncology/sarcoma preferred;
- Completion of a residency program and/or fellowship is preferred;
- Minimum of 5-7 years of medical affairs and/or development experience in the biotech/ pharmaceutical industry;
- Must have an in-depth understanding of medical affairs role and process;
- Ability to interact externally and internally to support global and regional business strategy;
- Proven leadership skills in matrix organizations and ability to bring out the best in others in cross-functional teams. Must be able to lead through influence;
- Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols;
- Must possess excellent oral and written English communication skills;
- Ability to exercise judgment and address complex problems and create solutions;
- Ability to build effective working relationships (internal/external), experienced in working in a matrix environment.
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