Edition du 18-11-2017


Medical Lead, Aflibercept and PD-1 en Oncologie ou Hématologie - Sanofi (IDF) CDI


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Medical Lead, Aflibercept and PD-1 en Oncologie ou Hématologie - Sanofi (IDF) CDI



Medical Lead, Aflibercept and PD-1 en Oncologie ou Hématologie - Sanofi (IDF) CDI - SANOFI

Sanofi est la 1ère entreprise de l'industrie pharmaceutique en France, avec 49 sites et 28 000 collaborateurs.


DateRecruteurFonctionLocalisationRéférence de l'offre
31-10-2017SANOFIMarketing - Communication France-IDF-Paris JO-R9824-MK-MYHARMA/ MPE-24523


Description de l’annonce emploi


Medical Lead, Aflibercept and PD-1 H/F SANOFI
CDI en IDF


Mission & Objective Description :


- To develop and implement the European Medical Plans for aflibercept and PD-1 aligned with the global medical strategies
- To interface with internal and external stakeholders to enhance the scientific and clinical understanding of the brands in the therapeutic area in agreement with Sanofi Genzyme internal compliance rules and regulations
- To provide scientific direction for the development of PD-1 and further investigation of aflibercept
- To create and execute pre-launch and launch strategies and activities around PD-1 in Europe
- To support Market Access activities and contribute in preparation and validation of the medical aspects of pricing and reimbursement dossier. Provide medical support to the countries in their negotiations with health authorities/drug evaluation institutions


Accountabilities/Responsibilities :
- European Medical Director will work in a leadership role within a cross-functional team of medical professionals around EU in planning and execution of all aspects of medical affairs relating to product support. This includes managing the scientific aspects, responsibility for creating strategies for European medical affairs, providing medical leadership into the marketing strategies, oversees execution of key publications and appropriate dissemination.
- Transversal cooperation with all departments (R&D, affiliates, legal, finance, regulatory, patent, global, marketing, BD, purchasing departments)
- Reviews, approves and supervises all aspects of EU medical affairs clinical trial program. Maintains approval of all protocols and conduct of all clinical studies in adherence to both Company standards and government industry regulations.
- Works closely with Regulatory e.g. in developing plans for submissions/extensions.
- Serves as interface between EU team and global franchise teams in coordinating medical activities, including helping in the development of global medical plans for the product.
- Is responsible for organizing core business team meetings, advisory board meetings, steering committee meetings
- Responsible for approval of EU related product promotional material, in compliance with corporate standards government industry regulations.
- Accountable for medical approval of all marketing and sales strategies and programs to ensure the highest degree of medical and ethical standards.
- Develops and maintains close professional relationships with top members/opinion leaders (physicians and researchers) within pertinent medical community. Fosters the establishment and maintenance of external scientific advisory boards and assists in advocacy development.


Requirements –Education and Experience


Educational background
Candidate is an MD with a preference for training at specialist level in Oncology or Hematology. Alternatively an MD with a proven track record in European medical affairs role in Oncology and/or Hematology for at least 5 years


Language skills
Strong verbal and written communication skills in English


Experiences and specific knowledge
Extensive experience (>5 years) in medical affairs functions in the Pharma business, ideally in oncology medical affairs. Experience working in a multi-country setting is a definite plus, as well as past international assignments.
Proven ability to engage, influence and build effective relationships with KOLs
Demonstrated experience in developing medical strategies and plans
Knowledge of the regulatory, compliance and legal framework


Professional competencies
Strategic thinking and prioritizing capacity
Patient-centred but commercially aware, values driven approach
Analytic, innovative and creative
Ability to translate data into a strategic medical plan


Behavioral competencies
Excellent influencing skills and negotiation/conflict resolution capabilities
Excellent presentation and influencing/negotiation skills
Comfortable operating in virtual teams
Intercultural savvy, good team player
High ethical standards required


Reporting Relationship
No direct line management/reports
Budget responsibility
Responsible for the creation, delivery and management of annual Brand Medical Budget


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