Vaccines & Antivirals Sr Medical Affairs Scientist

MAIN REPONSIBILITIES / 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.

Medical

LI-PFE