Experteer OverviewIn this role you provide medical, clinical and scientific guidance across IQVIA divisions to support trial delivery and business development. You act as a medical expert throughout the project lifecycle, ensuring protocol quality, patient safety and scientific rigor. You collaborate with cross‐functional teams, investigators and pharmacovigilance to translate medical insight into clinical trial success. This position offers impact in advancing therapeutic programs while shaping medical strategy and risk management. A global, 24/7 medical presence and travel readiness enable you to drive critical decisions in fast‐paced environments.Retribuzione / BenefitsServe as Global Medical Advisor on assigned projectsProvide scientific guidance to Project Leaders on medical and scientific aspectsSupport investigative sites and project staff on protocol-related issues including safety and eligibilityReview protocols, IDBs, and CRFs for medical accuracyDeliver therapeutic area training for the project teamAttend Investigator Meetings and present findingsReview trial-related Adverse Events (AEs) and, if applicable, Serious Adverse Events (SAEs) in collaboration with PharmacovigilanceSupport Analysis of Similar Events (AOSE) activities as neededReview adverse event coding and CSR/patient narrativesParticipate in Kick‐Off, team, and client meetingsBe available 24/7 for urgent protocol-related questionsMay travel 15%-20% of the timeResponsabilitàMedical Degree with license from relevant country/regionMinimum 5 years of clinical medicine experience and clinical trials experience as investigator or in pharma/CRO/biotechRobust knowledge of scientific, clinical, regulatory, and competitive landscape in applicable therapeutic areaKnowledge of applicable federal/local clinical research regulations and guidelinesBoard Certified in CardiologyKnowledge of cardiology, metabolic diseases and nephrologyExperience or knowledge in Phase I or early clinical developmentFluent in EnglishExcellent communication skills
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