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I&I – Senior Medical Affairs Scientist

2 meses atrás

Lisboa, Portugal Pfizer, S.A. De C.V Tempo inteiro

I&I – Senior Medical Affairs Scientist (Sr. MAS)The key responsibilities in this role include: Is responsible for the medical plans and execution of medical scientific strategic plans of the products assignedIs responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assignedIs responsible for all medical projects of the products assigned and the respective direct budget monitoringPerforms the Global Medical Grants (GMG) medical reviews and is the owner of medical studies and other data generation projects for the products assignedAligns, supports, and contributes to different internal stakeholders:collaborates and participates in working groups or other activities led by the Global and International Development Markets (IDM) Medical Teams for the assigned productsis the products' assigned medical point of contact for the cross-functional teams in the Business Unit (BU)provides medical input and medical strategic view to the Commercial area for the products assignedworks with Health&Value (H&V) in studies and reimbursement dossiers and is a participant of the Real World Life project's working groupscollaborates with Regulatory in all the activities in the products' lifecycle that require medical related input, review and/or approvalcollaborates with Supply Chain Quality (SCQ) in all the activities in the products' lifecycle that require medical related input, review and/or approvalcollaborates with Medical Information and Drug Safety Unit in special requests for which local medical affairs input or review is requiredcollaborates closely with all medical areas to ensure cross-pollination of best practices and innovative ideasis responsible for the internal medical training of all the assigned productsperforms ad-hoc promotional, non-promotional and medical-to-medical materials review and approvalperforms any other activity that requires medical input, review or approval for which is nominated by the Medical Team LeadIs a key contributor to ensure company's medical compliance in internal projects and external engagementsPerforms the medical customer facing activities for the assigned products, according to the priorities defined with the Manager, and liaises with the Medical Communication Colleagues, if applicableWorks closely with the MAS/Medical Communication, the MAS/Real World Data Expert, the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional team, including customer-facing rolesREQUIRED SKILL SET University Degree in health or life science areasMinimum of 2 years of experience in the Pharmaceutical Industry or in relevant healthcare sector activitiesProven experience in the following areas:Medical plans and budget managementMedical governance and cross-functional teams' collaborationMedical writing and comprehensive medical review of documentsCommunication skills to different stakeholders and across different channelsExternal engagement competencies, including networking and stakeholders mapping & managementPerformance driven with professional demeanor and strong collaboration skillsAbility to focus on priorities, resilience, organization, and project management competenciesSense of responsibility and accountability, quality orientationStrategic, agile, innovative and growth mindsetLanguage Requirements: Fluent in Portuguese and English
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