Medical Advisor, Oncology

c inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed
B. Operational: - Medical Initiatives/support for the Allocated Portfolio (New/Key Detail/In-line Products) - Provide strategic inputs and support towards creation of marketing/brand plans/medical development plans, and towards design and execution of medical-marketing programs/clinical programs, including initiatives to enhance access to medicines - Initiate and/or review and/or approve 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 are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, etc.

    **C. Clinical Research :**
-   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. In consultation with concerned stakeholder/vendor/interface, review and approve additional supporting documents/databases including ICF/CRF/SAP, etc.
-   Assist in planning, organizing and preparing Investigational New Drug Applications (NDAs)
-   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

D. Sales Force Training:

• Provide medical training to new sales staff on basic sciences/ TAs/assigned products. Provide refresher training to sales staff through ongoing training initiatives

• Provide pre-launch and launch training to sales staff for new products

  E. New Product Planning/Development:

• For global products, assist NPP team with preparing business case, and pre-commercialization programs/initiatives/activities to "prepare" internal and external stakeholders for new product launches. 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 opportunities to launch new products (e.g., licensing, acquiring, co-promotion, etc.)

• Support organization efforts at developing local formulations/line extensions through literature search/recommendations. Function as custodian for coordinating internal and regional approvals through the RFD (Request For Development) process

F. 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

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical