In this role you will serve as a global medical advisor and scientific expert across IQVIA divisions, guiding medical and scientific aspects of trials and business development. You will support investigators and project teams, review protocols and reports, and provide therapeutic area training. You’ll be involved in safety reviews, pharmacovigilance collaborations, and have 24/7 availability for urgent protocol questions, with regular travel. This is a high-impact position shaping clinical programs and patient outcomes within a leading CRO environment.
Act as Global Medical Advisor on assigned projects and provide strategic medical guidance to project leaders
Review protocols, IDBs, CRFs and CSR/patient narratives for medical accuracy and safety
Provide therapeutic area training to project clinical teams and present at Investigator Meetings
Review and clarify trial-related Adverse Events; participate in SAE case reviews with Pharmacovigilance
Support AOSE analyses and collaborate with Pharmacovigilance on safety signal assessment
Attend kickoff, weekly team, and client meetings; respond 24/7 to urgent protocol questions
Travel 15-20% as needed
Maintain up-to-date knowledge of scientific, clinical, regulatory, and competitive landscapes in applicable therapeutic areas
MD in Medicine with medical license appropriate to residence
minimum 5 years of clinical medicine experience plus clinical trials experience (investigator or within Pharma/CRO/Biotech)
Board Certified
experience or knowledge in Phase I or early clinical development
Fluent English with extensive communication skills
Knowledge of federal and local clinical research regulations and guidelines
ability to work across diverse teams and provide medical leadership
cross-functional collaboration
problem-solving
medical monitoring and safety review
pharmacovigilance collaboration
medical review of IDB/CRF/CSR
Associate Medical Director, Nephrology - barcelona barcelona, catalunya, es
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Associate Medical Director, Nephrology - Barcelona • Barcelona, Cataluña, Spain