Medical Oncology Benefit Advisor (M/F/X)

Medical Oncology Benefit Advisor (M/F/X)


Medical Oncology Benefit Advisor (M/F/X)

Dettagli della offerta

Daiichi Sankyo and its 15.000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In addition to a strong portfolio of medicines for hypertension and thrombotic disorders,the Group-s 2025 vision is to become a “Global Pharma Innovator with Competitive Advantage in Oncology”. Our European headquarters are in Munich, Germany and we have affiliates in 12 European countries. The Italian Affiliate is in Rome. For more information: . The position In your function you will supervise oncology benefit part and medical scientific projects as a medical- and benefit scientific expert and report directly to the Head of the Medical Department of Oncology. Key Responsibilities: Responsible for selection, coordination of medical content of the local reimbursement dossier Define the methodology to evaluate medical benefit and risk in coordination with other departments (market access and RRWE/HEORs, regulatory, patient safety, medical affairs) Responsible of the medical part of the local value dossier when it is applicable in line with the Market access department and regulatory department Coordinate and check the CSR and additional information with European and global teams Determine and plan, coordinate and check the setup of medical strategy to prepare the local value dossier with CRO involved To be the guarantor of methodological accuracy of medical part of the local value dossier and reimbursement dossier and local value dossier Set up and evaluate the relevance of epidemiological projects, registries, RWD generation to support the local value dossier To be the expert in the health environmental changes, guidelines, and local law regarding health authorities changes Create a network with KEEs to involve them in the local value dossier evaluation and contribute to the medical of the local value dossier To be part of payer-s ad board to present the medical data Help market access and other departments to choose the right KEE to be involved in value evaluation and to read the dossier Manage publication plan linked to RWD generation To be the medical expert for regulatory team when it is needed Give advice and support the cross functional team regarding methodology, scientific part and to go deeply in the existing data to support the local value dossier Medical activities: Responsible for medical-scientific projects and studies in the oncological field and medical customer service related to medical benefit activities Responsible to set up a local medical market access plan aligned with European and global strategic plan/vision in close collaboration with other involved departments Define the medical local strategy for pre-launch and launch products in collaboration with market access team Execute an external stakeholder plan with specific focus on stakeholders involved in guidelines and advisors to payers Participate to medical meetings at Europe level, give feedback and advices to implement medical strategy linked to benefit To be involved in patient drug access if applicable and to be a partner with the market access to ensure the drug access to the patient Set up competitive intelligence and follow new medical strategies, guidelines, environment changes and bibliographic review Support Medical Affairs clinical activities strategy, planning, design and execution (in close co-operation with HQ and CROs) with focus on health economy outcome measures Support the set up and follow up of registries and other non-interventional Medical Affairs studies Set up medical market access trainings if needed Work cross-functionally and collaborate with Market Access and other specialist functions like Marketing, PR, etc. Follow the budget for medical activities Cooperate at EU and global level Qualifications: Strong scientific background with completed studies preferably in the medical field of human medicine, pharmacy or human biology Several years of experience in a comparable position in the pharmaceutical industry or life science environment (e.g. as MSL) required Oncology knowledge mandatory Good understanding of local health economy environment and requirements for local value dossiers Risk / benefit awareness and environmental awareness Experienced in dealing with opinion leaders Good knowledge and experience in dealing with scientific studies and medical projects including the corresponding regulations Very good English and MS-Office skills Strong communication skills and presentation confidence High self-motivation, assertiveness and goal orientation Quick comprehension Good conceptual skills and the ability to present complex interrelationships Strong ability to work in a team "Hands on" mentality

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