Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

Experteer Overview

In this role you provide medical, clinical and scientific advisory support across IQVIA divisions, guiding project delivery and business development. You act as a medical expert for assigned trials, ensuring patient safety and scientific integrity throughout the study lifecycle. You will train teams, review study materials, and support regulatory and pharmacovigilance activities. The role offers exposure to global projects and cross-functional collaboration in a leading CRO environment.

Retribuzione / Benefits

• Serve as Global Medical Advisor on assigned projects and provide scientific guidance to project teams
• Support investigators and project staff on protocol-related issues, safety, and eligibility
• Review protocols, IDBs, and CRFs for medical accuracy
• Provide therapeutic area training to the project clinical team
• Attend Investigator Meetings and present clinical insights
• Review and clarify trial-related Adverse Events; participate in SAE case reviews with Pharmacovigilance
• Assist with AOSE analyses in collaboration with Pharmacovigilance
• Review adverse event coding and the Clinical Study Report and patient narratives
• Participate in Kick-Off, weekly team, and client meetings as needed
• Respond 24/7 to urgent protocol-related questions; travel 15–20% may be required

Responsabilità

• MD with medical license from the country/region of practice
• Minimum 5 years’ experience in clinical medicine and clinical trials
• Robust knowledge of scientific, clinical, regulatory, commercial, and competitive landscape in the therapeutic area
• Knowledge of federal/local clinical research regulations and guidelines
• Business acumen
• Board Certified in Cardiology
• Knowledge of cardiology, metabolic diseases, and nephrology
• Experience or knowledge in Phase I studies or early clinical development
• Fluent English and extensive communication skills