Sr Medical Affairs Scientist Oncology Pipeline
Pfizer
The Sr MAS Oncology Pipeline is an integral member of the Oncology Italy Medical Affairs organization and Medical Oncology Leadership Team. The Oncology category has been developed to maximize the existing in-line portfolio offering the scientific expertise and excellence while positioning Pfizer as Oncology category leader with an exciting and promising pipeline. Pfizer is a pioneering leader in the field of Oncology. We are committed to understanding the individualized treatment journey, the biology behind different cancers and identifying biomarkers, or genetic mutations, that can be targeted to inhibit cell growth. Today we are at the forefront of bringing these breakthrough biomarker-driven treatment options to patients through our precision medicines in lung cancer, melanoma, and colorectal cancer. The Sr MAS will join Oncology Medical Team and will be responsible for Pipeline in Italy. Will have direct relationships with healthcare professionals and research centers focused on increasing quality of partnerships to share the common final objective: patient’s health improvement. -Maintain the highest scientific standards during in/external activities to provide deep medical and scientific expertise -Work with MAS Line Managers Oncology and Global team to coordinate the relevant activities aimed at developing and increasing capability of customer facing and omnichannel approach including digital tools across Oncology Medical Team in Italy -Establish a strong collaborative scientific relationship with relevant stakeholders in the assigned area (KOLs, medical societies, and other relevant internal/external stakeholders) -Integrate customer medical insights into the country medical and brand strategy, provide medical and scientific strategic support to the regional medical team, medical leadership to the country brand team, country and / or local XFTs, drive implementation of the country medical plan. -Contribute to the implementation of local medical strategies and life cycle clinical plans for relevant TAs -Provide scientific and medical data to leading health professionals and decision-makers to ensure safe, proper, and effective uses of assigned products, contributing to patients (and populations) health and well-being -Observe compliance rules, ensuring activities and communications are conducted in compliance with all policies, guidelines, and regulation and ensure the respect of medical independence
Roma
Tue, 30 Jul 2024 22:49:20 GMT
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