Medical Advisor, Specialty Care

1. Strategic/Policy
• With support from the mentor or Line manager, provide tactical and strategic inputs, and medical expertise, to Product Management towards ethical promotion of assigned products

2. Operational
• Under supervision from the Line manager or the mentor, provide strategic inputs and support towards creation of marketing/brand plans/medical development plans, and towards design and execution of medico-marketing programs/clinical programs, including initiatives to enhance access to medicines
• Initiate and/or review promotional, training, and Continuing Medical Education (CME) material in compliance with relevant SOPs/regulations/industry codes/working practices
• Participate/facilitate/conduct customized promotional/educational interactions with Health Care Professionals (HCPs). These interactions include, but not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, etc.
• In consultation with concerned stakeholder/vendor/interface, develop/write and/or review and/or approve protocol synopsis/final protocols/supporting documents per need (e.g., investigators’ brochure (IB), informed consent form (ICF), patient information sheets, etc) for , Phase IV, PMS, Observational studies / surveys, Pharmacoeconomic / Outcomes Research studies, and other clinical projects / programs.
▪ Review/interpret data generated; write final reports for locally sponsored studies as required
▪ Develop and execute Publication Plan; review/approve/write manuscripts for publication of locally sponsored studies
▪ Develop and execute Information Dissemination Plan/Program

Medical Information

Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies

Sales Force Training
• Provide medical training to cross functional colleagues on basic sciences/ TAs/assigned products. Provide refresher training to sales staff through ongoing training initiatives

− New Product Planning/Development
• For global products, assist NPP team with preparing business case, and pre-commercialization programs/initiatives/activities for internal and external stakeholders. These include assistance with market research, stakeholder mapping, and early access programs
• Support New Product Planning, Marketing, and Business Development colleagues with medical evaluation and recommendations on commercial opportunities with new products (e.g., licensing, acquiring, co-promotion, etc.)
• Support organization efforts at developing local formulations/line extensions through literature search/recommendations.

− Regulatory
• Provide medical and product expertise towards registration of new products/indications with federal/state regulatory authorities through delivery of scientific presentations, provision of medical rationale and published literature, and liaison with key HCPs for obtaining support for new product/indication.
• Provide medical and product expertise towards defense of marketed products (regulators, NGOs, press, etc.)
• Write, revise, and review labeling documents for pipeline/local products per relevant SOPs
• Provide medical support towards processing of spontaneous/solicited AE reports, per relevant SOPs and/or working practices

3. Values and Behaviors:
• Consistently adhere to/demonstrate all Pfizer Values/Leadership Behaviors

QUALIFICATIONS

MBBS/ MD,

2-4 years of relevant experience in hemophilia, hematology/blood disorders

Experience of working with government and reimbursement accounts preferred,

Work Location Assignment:On Premise

Work Location Assignment: On Premise

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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Medical