About this role
Dr. Reddy’s Laboratories Ltd., a leading multinational pharmaceutical company, seeks a Medical Affairs Manager to drive new product launches in EM countries. Execute the Medical Affairs plan and provide strategic inputs to cross-functional teams including marketing, strategy, regulatory, portfolio, and clinical development. The purpose is to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
Day-to-day involves building relationships with global KOLs and supporting country teams to address HCP queries. Organize and lead scientific events like advisory boards, global webinars, and ISPs. Disseminate scientific updates on product and therapy area at internal and external meetings.
Collaborate across sales, marketing, portfolio, and strategy teams with scientific and clinical support. Review promotional materials, ensure compliance with SOPs and regulatory standards, and conduct training on disease area, product knowledge, and guidelines. Work in a discrimination-free environment as an equal opportunity employer nurturing diverse talent.
Support evidence generation through sponsored studies, real-world evidence, and publications. Gather customer insights and market trends to strengthen medical and commercial strategies. Contribute to future strategy development, portfolio expansion, and sustainability respecting people, planet, and purpose.
Requirements
- Expertise in medical strategy and planning for pharmaceutical product launches
- Experience building and maintaining KOL relationships globally
- Knowledge of scientific engagement through advisory boards and webinars
- Familiarity with evidence generation including real-world studies and publications
- Proficiency in reviewing promotional materials for regulatory compliance
- Ability to analyze market insights for strategy development
- Scientific communication skills for internal and external dissemination
Responsibilities
- 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
- Build and maintain relationships with a set of KOLs globally and support country teams to address HCP queries
- Organize and lead COE-driven scientific events such as advisory boards, global webinars, and ISPs
- Support DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance
- Review and approve promotional materials, events, FMV calculation, KOL tiering and ensure compliance with SOPs and regulatory standards
- Conduct training sessions for internal teams on disease area, product knowledge, guidelines, differentiation
Benefits
- Work environment free from discrimination
- Equal opportunity employer committed to diverse workforce
- Nurture qualified talent regardless of race, color, religion, nationality, sex, age, disability, genetics, sexual orientation, gender expression
- Purpose-driven culture focused on sustainability, people, planet, and transparency
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