ph3Job Overview /h3 pThe Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. /p h3Essential Functions /h3 h3Medical Monitoring /h3 ul liPrimarily serves as Global Medical Advisor on assigned projects. /li liServes as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects. /li liProvides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. /li liPerforms medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs). /li liProvides therapeutic area/indication training for the project clinical team. /li liAttends and presents at Investigator Meetings. /li liPerforms review and clarification of trial-related Adverse Events (AEs). /li liMay perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. /li liMay provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. /li liMay perform medical review of adverse event coding. /li liPerforms review of the Clinical Study Report (CSR) and patient narratives. /li liAttends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.



/li liAvailable 24/7 to respond urgent protocol-related questions from investigative sites, in accordance with local labor laws. /li liMay require regular travel (15%-20%). /li /ul h3Qualifications Requirements /h3 ul liMedical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, along with a medical license, or equivalent, from the country or region in which he/she resides and works is required, plus a minimum of 5 years' experience in clinical medicine, in addition to clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry. /li liRobust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. /li liKnowledge of applicable federal and local regulations and guidelines pertaining to clinical research. /li liBusiness Acumen. /li liBoard Certified in Cardiology. /li liKnowledge of cardiology, metabolic diseases and nephrology. /li liExperience or knowledge in Phase I studies or early clinical development. /li liFluent English. /li liExtensive communication skills. /li /ul h3Pay Range and Benefits /h3 pThe potential base pay range for this role, when annualized, is €73,900.00 - €125,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or tempo parziale). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. /p /p #J-18808-Ljbffr

📌 Associate Medical Director, Cardiology, with Metabolic Diseases and Nephrology Experience (Turbigo)
🏢 Iqvia
📍 Turbigo