Medical Advisor Job at Pfizer, Mumbai
Looking for a Medical Advisor job with a global pharmaceutical leader? If you are an MBBS or MD professional with experience in hematology, hemophilia, or blood disorders, this Medical Advisor Job in Mumbai is an excellent opportunity to join Pfizer as a Medical Advisor, Specialty Care. This role at Pfizer Careers involves providing strategic medical leadership, supporting product development, collaborating with healthcare professionals, and contributing to scientific and regulatory activities. Read on to explore the job details, responsibilities, qualifications, and benefits before applying.
About the Company:
Pfizer is one of the world’s leading research-based biopharmaceutical companies committed to discovering, developing, and delivering innovative medicines and vaccines that improve patient health worldwide. With a strong focus on scientific excellence, innovation, and patient care, Pfizer operates across multiple therapeutic areas and partners with healthcare professionals, researchers, and regulatory authorities to advance global healthcare.
Job Details:
- Job Title: Medical Advisor, Specialty Care
- Location: Mumbai, India
- Job Type: Full-Time
- Work Mode: On-Premise
- Department: Medical Affairs
- Therapeutic Area: Specialty Care
- Government/Reimbursement Account Experience: Preferred
Key Responsibilities:
Strategic & Policy Responsibilities
- Provide tactical and strategic medical inputs to Product Management for the ethical promotion of assigned products.
- Offer medical expertise to support strategic business decisions.
- Assist in developing medical development plans and brand strategies.
Medical Affairs & Operational Responsibilities
- Support the development and execution of marketing plans and medico-marketing programs.
- Assist in designing and implementing clinical programs and initiatives to improve patient access to medicines.
- Develop, review, and approve promotional materials, training content, and Continuing Medical Education (CME) materials in compliance with company SOPs and industry regulations.
- Participate in customer launch meetings, advisory boards, scientific symposia, institutional presentations, and educational programs for healthcare professionals.
- Collaborate with stakeholders to develop, review, and approve:
- Clinical study protocols
- Protocol synopsis
- Investigator’s Brochure (IB)
- Informed Consent Forms (ICF)
- Patient Information Sheets
- Support Phase IV studies, Post-Marketing Surveillance (PMS), observational studies, surveys, pharmacoeconomic studies, outcomes research, and other clinical projects.
- Interpret clinical data and prepare study reports.
- Develop publication strategies and review or write scientific manuscripts.
- Execute information dissemination programs for clinical evidence.
Medical Information
- Provide timely, balanced, accurate, and evidence-based medical information to:
- Internal sales teams
- Healthcare professionals
- Ensure compliance with relevant SOPs and organizational policies.
Sales Force Training
- Conduct medical training programs for cross-functional teams.
- Deliver product and therapy-area training.
- Organize refresher training sessions for sales personnel.
New Product Planning & Development
- Support business case preparation for global products.
- Assist in market research and stakeholder mapping.
- Support early access programs.
- Provide medical evaluation for licensing, acquisitions, co-promotion opportunities, and business development initiatives.
- Support development of local formulations and line extensions through scientific literature review and recommendations.
Regulatory Responsibilities
- Provide scientific support for product registration and new indications.
- Deliver scientific presentations to regulatory authorities.
- Liaise with healthcare professionals to support regulatory submissions.
- Support defense of marketed products before regulators and other stakeholders.
- Prepare, revise, and review labeling documents.
- Provide medical support for processing spontaneous and solicited adverse event reports.
Organizational Responsibilities
- Demonstrate Pfizer Values and Leadership Behaviors consistently.
- Collaborate effectively with cross-functional teams.
- Maintain high ethical and compliance standards.
Educational Requirements for the Medical Advisor Job:
- MBBS or MD from a recognized medical institution.
- Valid medical registration.
- 2–4 years of relevant experience in:
- Hemophilia
- Hematology
- Blood Disorders
- Experience working with government and reimbursement accounts is preferred.
Skills Required:
- Strong medical and scientific knowledge
- Clinical research understanding
- Medical affairs expertise
- Scientific writing and publication planning
- Clinical study management
- Regulatory affairs knowledge
- Pharmacovigilance awareness
- Medical communication skills
- Presentation and training abilities
- Stakeholder management
- Healthcare professional engagement
- Strategic planning
- Cross-functional collaboration
- Analytical and critical thinking
- Project management
- Ethical decision-making
- Excellent interpersonal and communication skills
Benefits of the Medical Advisor Job:
- Opportunity to work with a globally recognized pharmaceutical company.
- Exposure to cutting-edge therapies in Specialty Care.
- Involvement in strategic medical affairs and product development.
- Opportunity to collaborate with leading healthcare professionals and key opinion leaders.
- Participation in clinical research and publication activities.
- Professional growth through cross-functional collaboration.
- Exposure to regulatory and market access initiatives.
- Continuous learning and career development opportunities.
- Inclusive and diverse workplace culture.
- Equal opportunity employment with a strong focus on ethics and innovation.
