Ta Head New Products, Medical Affairs

vor 1 Woche


München, Deutschland Daiichi Sankyo Europe Vollzeit

The Head TA New Products (Medical Affairs) is responsible to proactively screen and evaluate new potential assets to be in-licensed to DSE SBD from a medical perspective, together with a x-functional team at DSE (Market Access and Commercial) and other global partners (especially BD, global medical affairs, global marketing, global strategy)

**Roles and Responsibilities**:

- Matrix lead of a x-functional team at Daiichi Sankyo Europe, driving in-licensing activities
- Lead of a small medical team with 1 to 2 direct reports
- Lead the search, triage and evaluation of in-licensing opportunities from biotech and peer-pharma, including early research projects, new modality platforms, pre-clinical and clinical stage assets and Life Cycle Management (LCM) opportunities
- Active participation and contribution into highest global R&D board, i.e. Global Portfolio and Asset Decision Committee (G-PAD)
- Establish and lead Due Diligence teams at DSE and process to drive the detailed scientific evaluation of potential assets to support recommendations at governance
- Prepare materials for senior management briefings of recommended opportunities
- Ensure effective communication during BD process with key internal partners and cross-functional teams
- Building and maintaining a broad network of internal and external partners
- Leveraging relevant database and analytics tools to curate technology and disease (target) biology maps in support of opportunity identification and prioritization, and anticipation of new entry points
- Support the evaluation of new database/analytics to improve upon curation of insights
- Conduct primary and secondary research in support of due diligence and/or strategic projects which may include, but is not limited to: KEE interfacing, medical/scientific congress attendance, review of scientific literature, and analyzing/tracking key competitors
- Producing a landscape assessment to give an idea of the current, and future, competitive dynamics of the disease space
- Provide recommendations for product improvements and enhancements

**Education & Professional Experience**:

- MD preferred, University degree in natural sciences (medicine, pharmacy, chemistry, biotechnology, biology or equivalent) followed by 15+ years of experience in relevant roles/positions
- Deep scientific and medical expertise in a broad field of disease areas, focus on cardiovascular and immunological diseases is a plus
- Previous experience in R&D throughout all phases and experience in planning a product life cycle management program
- Experience in Marketing Authorization Applications
- Experience on active participation in Due Diligence activities and processes is a plus
- Demonstrate creativity and practice change management in order to guarantee a continuous improvement
- Proven leadership skills in a matrix environment
- Show empathy, respect and fairness
- Live a culture of cooperation and team-work and take action to prevent and solve conflicts
- Ability to work independently and as part of a team
- Work proactively and encouraging others, show assertiveness and strong resilience
- Strong communication, negotiation and presentation skills
- Effective planning und review of projects
- Analytical and systematic thinking, problem solving and ability to drive medical decisions

**Why work with us?**:



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