Sr. Medical Affairs Scientist (MAS) Vaccines & IM - 6-month Secondment / Temporary ContractThe key responsibilities in this role include: Is responsible for the medical plans of the products assigned and its execution.Is responsible for all medical projects of the products assigned (including advisory boards, educational programs, etc.) 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, including real world evidence.Leads medical to medical communications and is the medical expert for Health Care Professionals (HCPs) and Medical Societies – is the key point of contact for external proactive and reactive medical interactions (face-to-face – F2F and digital) with selected HCPs. Has relevant medical-to-medical (M2M) discussions about the therapeutic area (including diagnostic and therapeutic guidelines), medical challenges and data gaps, patient education needs, healthcare environment and future trends in the respective medical field. Is responsible for organizing and conducting clinical sessions, as project owner, speaker, or moderator. Supports the commercial speakers' program initiatives by conducting speakers' briefings.Is the responsible for the development and continuous update of a stakeholder's plan (compliant with GDPR and Pfizer requisites) according to the medical specialties in scope.Timely creates up to date M2M content and tailored HCPs and patients' materials/solutions for F2F and digital interactions, approved through the adequate review & approval system. Is responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assigned.Provides timely update of the medical interaction tool, following up on the HCPs' questions/insights/topics of interest and ensuring a constant flow of M2M relevant discussions.Collaborates closely with all medical areas to ensure sharing of medical knowledge and cross-pollination of best practices and innovative ideas.Aligns, supports, and contributes to different internal stakeholders:
collaborates and participates in working groups or other activities led by the Global and Chief Medical Affairs Office (CMAO) 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 therapeutic area.provides medical input and medical strategic view to the Commercial area for the products assigned.works with Access&Value (A&V) in studies and reimbursement dossiers.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.is responsible for the internal medical training of all the assigned products.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.Works closely with the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional teams.REQUIRED SKILL SETUniversity 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.#LI-PFE 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!
#J-18808-Ljbffr