The Medical Advisor will provide scientific and medical support to external and internal customers in accordance with AbbVie policies, and local regulations. It will ensure peer-to-peer scientific exchange with different stakeholders that includes: Providing medical (scientific, informational) support for AbbVie products, clinical studies and projects in the area(s) of responsibilityProviding medical and scientific training and support for the field force in respective TAsExternal Experts’ engagementProviding input into local studies and any relevant marketing-medical programsProviding medical and scientific inputs to business unit, Market Access, Site Management and Monitoring, Regulatory and other departments as neededResponsibilities: 1.
Brand and In-field Plans development and executionProvide inputs in development BP and IFTP for respective TAs area in accordance with global guidance and country specific business needsIdentify relevant local evidence, clinical care and educational gaps and provide proposals to close2.
External Expert (EE) EngagementBuild, develop and maintain strong relationship with Key National and Regional Medical Scientific Thought Leaders and key external customersExecution of EE engagement plansScientific Communication and exchange (development printed materials, speaker training materials, symposia, advisory boards, AbbVie-sponsored lecture content)Ensure EEs involved in development clinical guidelines are aware of recent AbbVie Products` dataMedical content for Educational, Early Dx, and digital programsDevelop and execute publication planConduct Advisory Boards and Expert MeetingsManning medical booths at the congressesHandling medical information requestsInsights collections3.
Evidence generationEvaluate and discuss affiliate study concepts and proposalsSite Management and Monitoring team alignment to ensure adequate enrollment into AbbVie products’ studies4.
Working relationships, internal support and interactionBecome the expert for specific TAs and products in order to support internal customers, capable to work in synergistic way across functionsIdentify needs and provide trainings to commercial colleagues including updates for marketing people on the most important publications and its value for local operationsDevelop materials where it is relevant (scientific-based, not promotional)Maintain timely approval of promotional materials in accordance with the timelines established by the local SOPObjection handling and competitor readinessParticipate to Pharmacovigilance activities (PV)Provide necessary support to Regulatory activities: contribute in SMPC development, validation5.
Medical compliance and governanceAct with ethics & integrity; provide non-promotional, balanced, reliable and scientific information to HCP, follow strictly the local regulation regarding off label discussionsComply with both local and international law and regulations and code of practice (AIPM code, etc), AbbVie SOPs, corporate/country governance; attend and comply with corporate/specific trainingsMedical degree (M. D.
) is a plusScience degree is a plus3 years+ experience in the Pharma/Biotech industry as Medical AdvisorPrevious experience in respective TAs is a distinct advantageSkills to analyze and interpret scientific informationKnowledge of clinical development (clinical trials)Knowledge of local pharmaceutical regulations and related ethic behaviorsAbility to work efficiently – both individually and as part of a teamComputer skillsRequirements: Medical degree (M. D.
) is a plusScience degree is a plus3 years+ experience in the Pharma/Biotech industry as Medical AdvisorPrevious experience in respective TAs is a distinct advantageSkills to analyze and interpret scientific informationKnowledge of clinical development (clinical trials)Knowledge of local pharmaceutical regulations and related ethic behaviorsAbility to work efficiently – both individually and as part of a teamComputer skillsUpper-intermediate English
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