Devise strategies and planning for launch of new indication/ products including KOL engagement and medical education.
Drive real world evidence generation activities in close collaboration with affiliate medical colleagues, region, and global counterparts.
Liaise with the regional medical team to identify the need gaps and generate actionable insights.
Liaise with professional associations and KOLs to build and drive scientific advocacy for the product/ TA.
Drive medical education and scientific dialogue for products and therapy area in collaboration with cross functional teams.
Assisting regulatory personnel to ensure that all promotional activities, NNIPL products, and packaging conform to regulatory laws and guidelines.
Facilitating organizational readiness and external scientific advocacy for new product launches in close collaboration with regulatory and commercial teams.
Supporting clinical operations and regulatory teams in regulatory submissions, presentations, and approvals for indication expansions and new product approvals.
Qualifications
MBBS or MD/MS in pharmacology (desired) from a reputed institution with minimum 2 years of industry medical affairs experience preferably in Diabetes disease (NGI) management.
Strong scientific knowledge and interest in Diabetes and its products, good collaboration with internal and external stakeholders as well as good in communication.
Strong strategic and analytical capabilities, with demonstrated experience in analysing complex situations.
Skills for planning, execution and follow-up is required, with a creative and innovative attitude that will enable you to drive initiatives with operational excellence in mind.
