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As a Clinical Research Associate, you'll play a critical role in the successful execution of clinical trials across Argentina. You'll be the vital link between Novo Nordisk and clinical trial sites, ensuring that our studies are conducted with integrity, in compliance with integral standards, and with patient safety as the top priority.
Your responsibilities will include:
Monitoring clinical trial sites across Argentina to ensure compliance with ICH-GCP guidelines, study protocols, and regulatory requirements
Conducting site initiation, routine monitoring, and close-out visits at investigator sites
Reviewing and verifying source documents, ensuring data quality and integrity for submission to regulatory authorities
Building strong relationships with principal investigators, study coordinators, and site staff to support successful trial execution
Managing eTMF documentation and IVRS systems, ensuring accurate and timely data entry
Identifying and resolving site-level issues proactively, escalating when necessary




Traveling within Argentina approximately twice per month to visit clinical trial sites
Your new department
Within International Operations, Clinical Trials Operations is responsible for the operational execution of clinical studies that bring innovative treatments to patients. Our team works across diverse therapy areas, collaborating with investigators, healthcare professionals, and cross-functional partners to ensure every trial meets rigorous quality standards. Your work will directly contribute to expanding access to breakthrough medicines for patients living with serious chronic diseases.
Your skills & qualifications
We're looking for an experienced Clinical Research Associate who is passionate about clinical research and committed to patient safety. You'll bring with you:
University degree in Medicine, Pharmacy, Biotechnology, QFB (Chemical Pharmaceutical Biology) or related health sciences
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📌 CRA Jr. (Buenos Aires)
🏢 Novo Nordisk A/S
📍 Buenos Aires