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 assigned Is responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assigned Is responsible for all medical projects of the products assigned and the respective direct budget monitoring Performs the Global Medical Grants (GMG) medical reviews and is the owner of medical studies and other data generation projects for the products assigned Aligns, 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 products is 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 assigned works with Health&Value (H&V) in studies and reimbursement dossiers and is a participant of the Real World Life project’s working groups collaborates with Regulatory in all the activities in the products’ lifecycle that require medical related input, review and/or approval collaborates with Supply Chain Quality (SCQ) in all the activities in the products’ lifecycle that require medical related input, review and/or approval collaborates with Medical Information and Drug Safety Unit in special requests for which local medical affairs input or review is required collaborates closely with all medical areas to ensure cross-pollination of best practices and innovative ideas is responsible for the internal medical training of all the assigned products performs ad-hoc promotional, non-promotional and medical-to-medical materials review and approval performs any other activity that requires medical input, review or approval for which is nominated by the Medical Team Lead Is a key contributor to ensure company’s medical compliance in internal projects and external engagements Performs 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 applicableNegotiable University Degree in health or life science areas Minimum of 2 years of experience in the Pharmaceutical Industry or in relevant healthcare sector activities Proven experience in the following areas.
edical plans and budget management Medical governance and cross-functional teams’ collaboration Medical writing and comprehensive medical review of documents Communication skills to different stakeholders and across different channels External engagement competencies, including networking and stakeholders mapping & management Performance driven with professional demeanor and strong collaboration skills Ability to focus on priorities, resilience, organization, and project management competencies Sense of responsibility and accountability, quality orientation Strategic, agile, innovative and growth mindset Language Requirements.
Fluent in Portuguese and English Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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