The Medical Advisor provides support to the Therapy Area Lead / Medical Manager to develop the medical strategy on different portfolios in order to ensure the safe and effective use of GSK medicines, by supporting effective scientific interactions with Healthcare Professionals and professional associations.
The Medical Advisor also plays a role in providing the support to execute the medical affairs plans.
Minimum Level of Education
MBBS / BDS and 2-3 Years of Experience (Preferably in a similar role)
Area of Specialisation
Worked in specialty segments (preferably Primary Care / Anti-Infectives)
Skills & Knowledge
Excellent Communication and Presentation Skills
Candidate should be comfortable travelling and interacting with HCPs
Strong business Accumen and knowledge of Rx Industry is preferred
Support the Development of Medical Plans as part of the Business Plan
Support the exchange and dissemination of scientific, educational, and research related information.
Support Scientific Engagement Activities : Planning / organizing / supporting / participating in advisory boards / SE activities supervised by the Therapy Area Lead / Medical Manager.
Deliver talks for our promoted indications and other non-promotional activities.
Provision of the Medical Information : Responds to an unsolicited MI request for on- or off-label information about a GSK product or their specific therapeutic area for the assigned portfolios
Internal scientific support : Liaise with relevant commercial colleagues and also serve as an internal scientific and medical expert by selective support to training activities in addition to answering scientific / medical queries by the commercial colleagues.
Liaise with the Medical Operations department for the smooth execution of the relevant Medical Plans.
Upload / Review the commercial / medical material through Content Lab, ensure strong compliance with the code.
Collecting ISS ideas / Co ordination of ISS and KEG : when assigned, acts as a point of contact for investigators, facilitating the interface with investigators and local R & D department responsible for approval, and communication of study progress and completion / Life cycle management of the product.
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