Manager Medical Affairs, based at Gurugaon

Vvinayak Associates; Gurugram District; On-site; INR 4,000,000 - 7,000,000; Full time

Job summary

Vvinayak Associates in Gurgaon invites applications for Manager Medical Affairs to lead scientific strategy for allergen immunotherapy products. The role requires MBBS with MD in Pharmacology and 5+ years of relevant experience, with exposure to regulatory and pharmacovigilance functions.

The candidate will shape medical plans, engage KOLs, oversee CME activities, monitor scientific evidence, and support product launches within a multinational setting.

Qualifications

• MBBS with 5+ years of relevant experience.
• MD in Pharmacology with 3 years of relevant experience.

Responsibilities

• Develop and execute the annual Medical Affairs strategy aligned with global and local objectives.
• Provide scientific leadership across allergen immunotherapy and allergy diagnostics portfolio.
• Support lifecycle management and launch readiness for new products; identify unmet medical needs.
• Identify, segment, and develop relationships with national and regional KOLs and specialists.
• Develop and execute KOL engagement plans and organize Expert Panels and Scientific Round Tables.
• Develop and deliver medical education programs, CME, webinars, and educational materials.
• Represent company at national and international scientific conferences and congresses.
• Monitor emerging evidence and market trends; gather customer insights for evidence generation.
• Provide medical review for regulatory submissions and support pharmacovigilance activities.

Skills

KOL engagement

Scientific leadership

Medical communications

Education

MBBS

MD in Pharmacology

Job description

Greetings from Vvinayak Associates !

Manager Medical Affairs, based at Gurgaon for German MNC for Allergen Immunotherapy (Respiratory Allergies)

We are looking for a candidate with below Qualification ONLY

MBBS = 5+ years of relevant experience

MD in Pharmacology with 3 years of relevant experience.

PFB JD

Medical Strategy & Scientific Leadership

• Develop and execute the annual Medical Affairs strategy aligned with global and local business objectives.
• Prepare annual medical operational plans, budgets, and scientific priorities.
• Provide scientific leadership across the allergen immunotherapy and allergy diagnostics portfolio.
• Support lifecycle management and launch readiness for new products. Identify unmet medical needs and recommend scientific initiatives to support business growth.
• Provide medical input into strategic business planning and portfolio decisions.

Key Opinion Leader (KOL) & Scientific Engagement

• Identify, segment, and develop relationships with national and regional KOLs, allergy specialists, pulmonologists, ENT specialists, pediatricians, dermatologists, and immunologists.

• Develop and execute KOL engagement plans.
• Conduct scientific discussions and exchange with healthcare professionals.
• Organize Advisory Board Meetings, Expert Panels, and Scientific Round Tables.
• Capture medical insights to support product strategy and evidence generation.
• Build collaborations with academic institutions and research organizations

Medical Education & Scientific Communication

• Develop and execute medical education programs for healthcare professionals.
• Design and deliver Continuing Medical Education (CME) programs, scientific workshops, webinars, and educational meetings.
• Prepare scientific presentations, slide decks, training modules, and educational materials.
• Represent company at national and international scientific conferences and congresses.
• Support development of disease awareness initiatives and patient education programs.

Market Insights & Competitive Intelligence

• Monitor emerging scientific evidence and treatment guidelines.
• Track competitor products, publications, congress activities, and market trends.
• Gather customer insights from scientific interactions.
• Support business decisions through evidence-based medical intelligence.

Regulatory Affairs & Pharmacovigilance Support

• Provide medical review and scientific support for regulatory submissions.
• Support preparation and review of Product Information (PI), Package Inserts, Summary of Product Characteristics (SmPC), educational materials, and risk management documents.
• Collaborate with Regulatory Affairs during product registration and lifecycle management.
• Support pharmacovigilance activities, including medical assessment of adverse events where applicable.
• Ensure compliance with CDSCO, NDCT Rules, and global pharmacovigilance requirements.