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

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Required Skills