Vaccines & Antivirals – Sr Medical Affairs Scientist (Sr. MAS) - 2 positions The key responsibilities in this role include:
Responsible for the medical plans and execution of medical scientific strategic plans for the assigned products.
Responsible for the scientific content creation for the omnichannel strategy defined for the assigned products.
Responsible for all medical projects of the assigned products and the respective direct budget monitoring.
Perform Global Medical Grants (GMG) medical reviews and own medical studies and other data generation projects for the assigned products.
Align, support, and contribute to different internal stakeholders:
Collaborate and participate in working groups or other activities led by the Global and International Development Markets (IDM) Medical Teams for the assigned products.
Act as the medical point of contact for cross-functional teams in the Business Unit (BU) for the assigned products.
Provide medical input and strategic view to the Commercial area for the assigned products.
Work with Health&Value (H&V) in studies and reimbursement dossiers and participate in the Real World Life project's working groups.
Collaborate with Regulatory in all activities in the product lifecycle that require medical-related input, review, and/or approval.
Collaborate with Supply Chain Quality (SCQ) in all activities in the product lifecycle that require medical-related input, review, and/or approval.
Collaborate with Medical Information and Drug Safety Unit in special requests requiring local medical affairs input or review.
Collaborate closely with all medical areas to ensure cross-pollination of best practices and innovative ideas.
Responsible for the internal medical training of all assigned products.
Perform ad-hoc promotional, non-promotional, and medical-to-medical materials review and approval.
Perform any other activity requiring medical input, review, or approval as nominated by the Medical Team Lead.
Key contributor to ensure company's medical compliance in internal projects and external engagements.
Perform medical customer-facing activities for the assigned products, according to priorities defined with the Manager, and liaise with Medical Communication Colleagues, if applicable.
Work closely with MAS/Medical Communication, MAS/Real World Data Expert, Medical Quality Governance Manager (MQGM), Compliance, Legal, and all cross-functional teams, including customer-facing roles.
REQUIRED SKILL SET
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:
Medical 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.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
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