Global Medical Affairs Manager

OverviewThe Global Medical Affairs Manager is part of the Medical Affairs Team and represents the nexus of cutting-edgemedical and scientific insights with internal and external stakeholders contributing to drive medical innovation inthe therapeutic areas of competence and throughout the entire product life cycle.Reporting to the Global Medical Affairs Lead, he/she is in charge for active and value-adding scientificcontributions to cross-functional teams internally and engagement with key external stakeholdersMain Activities & ResponsibilitiesServe as the primary scientific and medical expert for the assigned therapeutic area/productswith internal and external stakeholders.Participate as representative of Global Medical Affairs in Global Project Teams/ Global BrandTeam.Contribute to the development and execution of the Global Medical Affairs Plan according tostrategic company milestones and budget.Work closely with internal stakeholders to execute that all activities in the Medical Affairs plandesigned to meet shared objectives are implemented and performed in a timely manner.Contribute to marketing strategies with scientific input and collaborate on organizing medicalevents.Provide impactful feedback/information to internal stakeholders on emerging clinical andscientific trends from external interactions to help shape company research and to ensure thesafe and appropriate use of Menarini Group products.Build specific excellence and integrity within the healthcare community. Develop contacts withkey clinicians, patient’s association and other medical/scientific groups.Contribute to Mapping of Key Opinion Leaders (KOLs) on the disease and KOLs insights on theproduct.Analyze, synthesize, and present medical scientific information in a structured way.Prepare and deliver training sessions on therapeutic areas and assigned products.Assist in the development and execution of clinically relevant medical meetings (e.g., advisoryboards, consultancy and investigator meetings), as requested.Contribute to planning, coordination, and presentations at global and national advisory boardsand other meetings.Contribute to publication planning, delivery, and disseminationContribute to the development and implementation of key international congressesDevelop, review and approve responses to unsolicited requests for medical information in linewith company’s SOPs and code of practice.Develops, review and approve promotional and educational materials for the allocatedtherapeutic area.Act as Study Medical Expert in the development of studies from initiation until publication andevaluate initiated investigator studies in the correspondent therapeutic area.Interact with key medical societiesSupport and review of grants for scientific projects in collaboration with clinical operationsProvides support and input into regulatory authority interactions, for example RMPs, PSURs,defending risk/benefit, Product Information.Provides support and input into early phase or market access aspects of clinical developmentplans.Contribute to developing SOPs and Working Instructions to improve efficiency, quality andcompliance in processes.Coordinate approval of contracts for external (consultancy/speaker) activities with HCPs or otherthird parties.Collaborate with external providers in different activities according to the Menarini Groupcode of practice and policies.Ensure all medical projects, materials and presentations are compliant to pharmaceutical codes.Act within compliance and legal requirements as well as within company guidelines.Other duties as assignedJob RequirementsEducation (Medical Doctor Degree)Years of experience (≥2 )Language skills and level of proficiency (Business fluency in English, both spoken and written)Other skills:Good verbal and written communication skills.Strong organizational, and cross-functional collaboration skills.Driven by Learning & Personal DevelopmentAbility to effectively collaborate in a dynamic and global environment.