Fr Msl Oncology Ile de France

**Passion for Innovation. Compassion for Patients.**:
With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world. In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life. In Oncology, we strive to become a global pharma innovator with competitive advantage, creating novel therapies for people with cancer. Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada.

**The position**:

- You will be the therapeutic area Oncology scientific expert, responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of leading specialists (physicians, pharmacists, hospital managers, board members of scientific societies, and other stakeholders).
- Considered as a trusted scientific counterpart and partner, you will maximize company product value through high scientific quality communication with leading specialists.
- Through activities in line with the Medical Affairs Plan in collaboration with our partner AZ, you will be jointly responsible for achieving short-term company goal.

**Key responsibilities**:

- Develop and execute an external stakeholder management plan in close collaboration and coordination with the respective cluster organizations in Medical Affairs, Commercial and Market Access (mainly in Lung & GI Cancer indications).
- Through scientific interactions, communicate the value of company products, champion the medical value of our oncology pipeline products fairly based on the risk-benefit profile of our drugs and contribute to the fostering of innovative approaches
- Represent the company to other therapeutic area stakeholders including professional associations and patient organisations in cooperation with other Medical functions
- Proactive and reactive communication of medical scientific data to leading specialists and broader external health-care related audiences
- Communicate non-promotional general information about our company, including pipeline, research and development programs and other relevant information
- Respond to unsolicited scientific queries from customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents
- Organization and participation in medical education activities: identify/support/educate speakers
- Act as a reference point for Market Access and Commercial functions for any scientific query, in collaboration with Medical Information as appropriate
- Support and manage Medical Affairs clinical activities strategy, planning, design and execution (in close co-operation with HQ and CROs)
- Support the set up and follow up of registries and other non-interventional Medical Affairs studies
- Propose investigators and sites for interventional and non-interventional Medical Affairs studies
- Manage field based medical projects
- Ensure a link between HQ, Regional Medical Dept. and KOLs
- Contribute the pre-launch and launch steps of new products providing scientific support
- Represent DS at medical meetings, conferences, advisory boards, and at key institutions, in interaction with KOLs
- Support medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy
- Assist with the scientific review, development, approval, execution and communication of affiliate medical affairs sponsored or supported clinical research activities.
- Visit Key Accounts and KOLs to answer any medical/scientific questions concerning the company’s molecule
- Ensure budgets, timelines, compliance requirements are factored into programs' scientific activities.

**Qualifications**:

- Scientific or medical degree (at least a 5 years higher education diploma : MD, PhD in medical/biological sciences or equivalent with relevant therapeutic specialty in an academic or hospital environment in oncology)
- Currently working in the field of oncology
- Experience in the biotech/pharmaceutical industry
- Strong understanding of the pharmaceutical business
- In-depth understanding of MSLs role and process
- Proven leadership skills in a cross-functional team environment
- Strong team player, ability to work independently
- Ability to interact externally and internally to support the business strategy
- Good knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols
- Very good english and MS-Office skills
- French native speaker

**Why work with us?**: