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Clinical Trials OperationsBuenos AiresJoin Novo Nordisk's Talent Pipeline!
Help bring life changing treatments to patients across Argentina by ensuring clinical trials are conducted to the highest standards of quality and compliance.Your new roleAs 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 general 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 requirementsConducting site initiation, routine monitoring, and close-out visits at investigator sitesReviewing and verifying source documents, ensuring data quality and integrity for submission to regulatory authoritiesBuilding strong relationships with principal investigators, study coordinators, and site staff to support successful trial executionManaging eTMF documentation and IVRS systems, ensuring accurate and timely data entryIdentifying and resolving site-level issues proactively, escalating when necessaryTraveling within Argentina approximately twice per month to visit clinical trial sitesYour new departmentWithin 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 & qualificationsWe'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 sciencesMinimum 2 years of proven experience as a CRA monitoring clinical trialsIntermediate to advanced English proficiency (written and spoken)Solid working knowledge of ICH-GCP guidelines, Argentine regulatory framework, and clinical trial platforms including eTMF and IVRSAvailability to travel within Argentina approximately twice per monthStrong attention to detail, organizational skills, and ability to manage multiple sites simultaneouslyExcellent interpersonal and communication skills to build effective relationships with site personnel

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📌 Clinical Research Associate - Talent Pipeline (Buenos Aires)
🏢 Novo Nordisk A/S
📍 Buenos Aires