Medical Affairs Job at Dr. Reddy’s Laboratories in Hyderabad
Looking for a Medical Affairs Manager job in Hyderabad in the pharma industry? Dr. Reddy’s Laboratories is hiring a Medical Affairs Manager specializing in Oncology and Hematology. This Medical Affairs Job in Hyderabad focuses on driving product launches and medical strategies across emerging markets. Candidates will work on scientific engagement, research insights, and evidence-based communication. It is an excellent opportunity for experienced medical professionals in medico-marketing. Apply now to be part of a global pharmaceutical leader.
About Dr. Reddy’s Laboratories:
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company with a presence in 66 countries. Established in 1984, the company has grown into a global organization with over 24,000 employees. It focuses on providing affordable and innovative medicines with a mission that “Good Health Can’t Wait.”
The company emphasizes research, sustainability, and patient-centric healthcare solutions. With a strong commitment to diversity, inclusion, and innovation, Dr. Reddy’s aims to reach over 1.5 billion patients worldwide by 2030. It maintains a work environment free from discrimination and promotes equal opportunity employment.
Job Details:
- Location: Hyderabad
- Department: Medical Affairs & Information
- Job Role: Manager – Medical Affairs (Oncology and Haematology)
- Function: GG EM (Emerging Markets)
- Experience Required: Minimum 3+ years in medico-marketing
- Employment Type: Full-time
Purpose of the Medical Affairs Job:
- Drive new product launch excellence and medical execution for priority oncology and haematology brands across Emerging Markets (EM) for Dr. Reddy’s Laboratories (DRL).
- Provide strategic growth levers and scientific insight for new and existing key products by translating clinical and real-world evidence into clear value narratives and practical field/commercial application.
- Enable high-impact scientific engagement (international speaker programs/ISP-CME, webinars, advisory boards, and in-country KOL visits) to strengthen scientific exchange and evidence utilization.
- Provide guidance and enablement to country teams for RWE generation and pharmacoeconomic/HEOR planning to support market access readiness.
- Ensure compliant execution through timely approvals and governance for scientific/promotional materials and external engagements in line with internal processes and applicable regulations.
Roles & Responsibilities:
New product launch excellence (Oncology & Haematology, Emerging Markets)
Own medical launch preparedness and execution support for new and key products across EM geographies, translating global strategy into country-ready launch plans.
Provide proactive scientific and strategic guidance to cross-functional and country teams to enable strong launch readiness, adoption, and growth levers for priority brands.
KOL engagement, speaker programs, and scientific exchange
Plan and deliver high-impact international and in-country scientific engagements including ISP/CME programs, webinars, advisory boards, and structured KOL visits.
Enable and coordinate KOL interactions to support evidence communication and appropriate utilization of data in clinical practice and medical education.
Country guidance & enablement; RWE and pharmacoeconomic planning
Provide guidance, governance and decision support to country medical teams for RWE generation, and pharmacoeconomic/HEOR planning.
Support development of country-specific medical plans, study concepts, and evidence roadmaps to strengthen payer, access, and clinical value narratives.
Scientific communications and medical content excellence
Create high-quality, visually strong scientific updates and post-congress evidence summaries on key products.
Synthesize data into clear field and commercial/strategic application, improving internal readiness and evidence utilization.
Launch preparedness support via training and tools
Develop and deliver medical decks, FAQs, and training modules; conduct country-team trainings to strengthen team capabilities.
Compliance approvals and governance
Ensure timely, high-quality compliance reviews and approvals for scientific/promotional materials and external engagements (e.g., ISP/CME, webinars, advisory boards, speaker nominations, FMV inputs, HCP classification/eligibility) in line with internal processes and applicable regulations.
Qualification and Key areas of Expertise:
- MBBS and MD with Pharmacology or Medicine with overall experience of ≥3 years in medico-marketing function, preferably with exposure to oncology/haematology
- Past experience of conducting KOL interactions/ Advisory Board meetings/ CMEs with thought leaders
- Experience of real-world clinical studies is desirable
- In-depth understanding about various cancers and principles of cancer therapy including latest products as well as upcoming treatment options and therapy modalities
Behavioral attributes
- Extrovert, proactive and self-driven, eager to connect with key stakeholders/external customers
- Good interpersonal relation skills with very good command on written and spoken English
- Good presentation skills along with good command of MS Office (PowerPoint, Excel and Word)
- Is team player and can work in diverse teams of cross function and lead the discussions
- Self-motivated and self-disciplined who can work to complete the projects / tasks within timelines
Benefits of the Medical Affairs Job:
- Personalized learning and career development programs
- Competitive industry-standard benefits
- Joining and relocation support
- Family support including maternity and paternity benefits
- Medical and life insurance coverage
- Opportunity to work in a diverse and inclusive environment
- Exposure to global pharmaceutical markets and innovation
