MAIN RESPONSIBILITIES / DUTIES
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 applicable.
Works 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 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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