Opportunity to work as Senior Medical Advisor @ Pfizer Inc - Mumbai City, India
Responsibilities
Job Purpose:
To actively contribute to the organization/business unit (BU)/TA cluster by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors. To lead the BU medical team in all activities medically related to the allocated Pfizer Business Unit portfolio and provide high quality and timely service in the areas of Product Commercialization/Promotional Support, Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, Medical Information, and Performance/People Management, and business support in the areas of New Product Development/ Branded Value Offerings, Regulatory Affairs, Quality Standards, and Business Technology .
Position Responsibities:
1. Strategic/Policy
a. Provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical
promotion of assigned products, in the operational areas listed
2. Operational
⢠Commercialization/Promotion of 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. ⢠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 ⢠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 ⢠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 commercialization. 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. Function as custodian for coordinating internal and regional approvals through the RFD (Request For Development) process ⢠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
Skills / Knowledge / Qualification / Experience :
1. Qualification & Experience
a. Postgraduates in Medicine with minimum 2 years of medico marketing / RMA experience.
b. Postgraduates in Medicine with at least one year of previous clinical research or clinical practice experience along with at least 18 months of Medico-marketing experience.
c. Graduates in Medicine with minimum 4 years of medico marketing / RMA experience.
d. Graduate in Medicine with at least one year of previous clinical research or clinical practice experience or other relevant experience along with at least 3 years of medico-marketing experience.
2. Special Skills & Knowledge
⢠Basic knowledge of pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines
⢠Knowledge of "pharmaceutical medicine" including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics and relevant Therapeutic Area/Products
⢠Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct
⢠Communication skills, both written and verbal (including medical writing and presentation skills)
⢠Analytical skills and reasoning, and sound medical judgment/decision making
⢠Interpersonal skills, internal & external networking and the ability to impact and influence
Click here to apply
Responsibilities
Job Purpose:
To actively contribute to the organization/business unit (BU)/TA cluster by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors. To lead the BU medical team in all activities medically related to the allocated Pfizer Business Unit portfolio and provide high quality and timely service in the areas of Product Commercialization/Promotional Support, Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, Medical Information, and Performance/People Management, and business support in the areas of New Product Development/ Branded Value Offerings, Regulatory Affairs, Quality Standards, and Business Technology .
Position Responsibities:
1. Strategic/Policy
a. Provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical
promotion of assigned products, in the operational areas listed
2. Operational
⢠Commercialization/Promotion of 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. ⢠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 ⢠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 ⢠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 commercialization. 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. Function as custodian for coordinating internal and regional approvals through the RFD (Request For Development) process ⢠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
Skills / Knowledge / Qualification / Experience :
1. Qualification & Experience
a. Postgraduates in Medicine with minimum 2 years of medico marketing / RMA experience.
b. Postgraduates in Medicine with at least one year of previous clinical research or clinical practice experience along with at least 18 months of Medico-marketing experience.
c. Graduates in Medicine with minimum 4 years of medico marketing / RMA experience.
d. Graduate in Medicine with at least one year of previous clinical research or clinical practice experience or other relevant experience along with at least 3 years of medico-marketing experience.
2. Special Skills & Knowledge
⢠Basic knowledge of pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines
⢠Knowledge of "pharmaceutical medicine" including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics and relevant Therapeutic Area/Products
⢠Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct
⢠Communication skills, both written and verbal (including medical writing and presentation skills)
⢠Analytical skills and reasoning, and sound medical judgment/decision making
⢠Interpersonal skills, internal & external networking and the ability to impact and influence
Click here to apply
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