Key Responsibilities: * Medical Strategy & Planning
Execute the Medical Affairs plan for DRL new product launch in EM countries
Provide strategic inputs to cross-functional teams including marketing, strategy, regulatory, portfolio and clinical development
Support the creation of target patient profiles, CLM contents and contribute to product differentiation strategies
Scientific Engagement & Communication
Build and maintain relationships with a set of KOLs globally and support country teams (MSL/ commercial) to address HCP queries
Organize and lead COE-driven scientific events such as advisory boards, global webinars, and ISPs
Disseminate scientific updates at internal and external meetings on product and therapy area
Evidence Generation & Publications
Support DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance, as and when required
Contribute to scientific publications, conference proceedings, and subsequent development of HCP communication on those studies
Other Core Internal and Administrative Support
Review and approve promotional materials/ events/ FMV calculation/ KOL tiering and ensure compliance with SOPs and regulatory standards
Conduct training sessions for internal teams (MSLs/ commercial) on disease area, product knowledge, guidelines, differentiation etc. at regular interval
Provide scientific and clinical support to sales, marketing, portfolio and strategy teams
Market Insights & Future Strategy Development
Gather and analyse customer insights and market trends to further strengthen medical and commercial strategies
Evaluate new products and provide medical rationale for portfolio expansion in related disease area
Support digital content creation, review, and approval for DRL platforms and leverage technology for scientific exchange and stakeholder engagement
Qualifications Required Qualifications:
MBBS + MD Pharmacology from a recognized medical institute in India
Minimum 2 years of experience in Medical Affairs in pharmaceutical industry
Must have prior experience in handling products in Diabetes and Cardiovascular therapy areas, preferably launching injectables and/or novel entities
Good understanding of clinical research, medical statistics, regulatory standards, and therapeutic area expertise
Excellent English communication, presentation skills, and project/stakeholder management skills.