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Medical Advisor -Oncology

2+ years
Not Disclosed
10 Dec. 27, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Job Title: Medical Advisor

Role Overview:
The Medical Advisor is a key contributor to Pfizer’s organizational objectives, ensuring the scientific, technical, and ethical integrity of all policies and initiatives. This role leads the medical team for the assigned Business Unit (BU) portfolio, delivering timely and high-quality support across various domains. These include medical initiatives, HCP interactions, CME, clinical research, sales force training, medical information, and performance management. The Medical Advisor also provides support in new product development, regulatory affairs, quality standards, and business technology.


Key Responsibilities

A. Strategic/Policy

  • Offer tactical and strategic insights to Product Management to ensure the ethical promotion of assigned products.
  • Contribute technical and business expertise to BU and TA clusters to achieve portfolio objectives.

B. Operational

Medical Initiatives and Portfolio Support

  • Provide strategic input for creating marketing and medical development plans.
  • Design and execute medical-marketing programs and clinical initiatives to enhance medicine access.
  • Review and approve promotional, training, and CME materials in compliance with industry standards and SOPs.
  • Facilitate HCP interactions, including advisory boards, symposia, CME programs, and institutional presentations.

C. Clinical Research

  • Develop, review, and approve clinical protocols, patient information sheets, and other supporting documents for Phase IV, PMS, and observational studies.
  • Assist in planning and preparing regulatory submissions, including Investigational New Drug Applications (NDAs).
  • Analyze and interpret clinical data, authoring final reports for locally sponsored studies.
  • Develop and execute publication and information dissemination plans.
  • Review and approve manuscripts and other scientific publications.

D. Medical Information

  • Deliver accurate, timely, and balanced medical information to internal teams and HCPs in compliance with policies and SOPs.

E. Sales Force Training

  • Provide medical training to sales staff on therapeutic areas and assigned products.
  • Conduct pre-launch and launch training for new product introductions.
  • Deliver refresher training through ongoing initiatives.

F. New Product Planning and Development

  • Support global and local teams in preparing business cases and pre-commercialization activities, including market research and stakeholder mapping.
  • Provide medical evaluations and recommendations for licensing, co-promotion, and acquisition opportunities.
  • Facilitate internal approvals for local formulations and line extensions through the RFD process.

G. Regulatory Affairs

  • Provide medical expertise for the registration of new products and indications, including liaising with HCPs and delivering scientific presentations.
  • Defend marketed products against regulatory, NGO, and media challenges.
  • Author and review labeling documents for pipeline and local products.
  • Support the processing of adverse event (AE) reports in compliance with SOPs.

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

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