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Functional Tasks

• Being at a local level, the Medical responsible of the specific Therapeutic Area, providing medical/ expertise, scientific support to Commercial, interact with the relevant stake holders, implementation of the local Clinical Program.
• Provide to healthcare professionals and decision makers accurate, unbiased, balanced, and timely answers to requests for information about our products
• Establish & manage scientific/clinical relations with KTL
• Actively participate in key medical and scientific conferences by staffing medical information booths, gathering intelligence on competitors and critically observing Merck-sponsored speakers
• Lead the Medical Strategy, drive the Local Clinical Plan facilitate the submission of IST, publications and assist in site selection for CR&D clinical projects
• Contribute to strategic decisions regarding Merck products where appropriate
• Deputy Medical Director to review and approve promotional / non promotional materials
• Collaborate with the LDSO regarding the reports of adverse events related to assigned products
• Proponent/ approver for the QUANTUM approval process for medical initiatives
• Ensure operational excellence by sharing best practices
• Proactively coordinates field need for medical/scientific knowledge required for management and support of company products and relative disease states (both in-line products and products in development)
• Implementing medical initiatives such as: Advisory Boards, Medical Booths, and Educational Events etc.)
• Works closely with the sales leadership to ensure optimal alignment of field resources in delivering therapeutic area goals and objectives in a compliant manner
• Ensures the development and execution of the medical operational plans for a brand/s in collaboration with commercial team
• Perform due diligence activities: medical evaluation of in-licensing offers for local products
• Support evaluation of medically local product development projects
• In collaboration with regional therapy experts and country medical director, is responsible for developing and managing a Key Opinion Leader development plan according to responsible therapeutic area goals, objectives and tactics
• Attends appropriate scientific meetings to maintain his/her awareness of research activities within therapeutic area
• Presents monthly updates to applicable cross-functional partners and therapeutic business reviews at Medical Affairs Internal Management Team Meetings as requested
• Manages field-based project responsibilities if applicable
• Acts as the Local Pharmacovigilance Responsible Person (LPVR). Refer to the attached Role Description.
• Perform QC verification on the accuracy of translated medical information between local language and English for relevant safety documents
• Pharmacovigilance and Medical Information: Act as the Local Pharmacovigilance and Medical Information Responsible Person (LPVR)