**Job Overview** Perform clinical research procedures and support study execution by collecting, recording, and interpreting data for participants enrolled or being screened for clinical studies. Ensure all activities follow study protocols, SOPs, and GCP guidelines. Contribute to daily workload planning and site operations. **Essential Functions** + **Support investigators** in preparing for and conducting clinical studies + **Review study materials** , including protocols, CRFs, and EDC systems + **Participate in study meetings** and maintain study-related communication + **Prepare and submit regulatory and ethics documentation** (FDA and other authorities) + **Recruit, screen, and orient study participants** ; maintain screening logs + **Create and maintain source documents** aligned with protocol requirements + **Schedule and conduct study visits** and perform protocol‑required procedures + **Collect and manage study data** ensuring accuracy, completeness, and compliance + **Handle laboratory activities** , including specimen preparation and logistics + **Monitor participant safety** and report adverse events appropriately + **Respond to participant inquiries** and resolve study‑related issues + **Join daily huddles** to align tasks and maintain operational standards + **Assist with data quality checks** and query resolution + **Perform complex clinical procedures** (ECG, sample collection, spirometry, vitals, dose verification, cannulation, telemetry monitoring) + **Document and interpret study findings** to support database development + **Support investigators** in meeting study timelines, budgets, and regulatory requirements + **Train new site staff** and maintain training documentation + **Prepare for monitoring visits, audits, and regulatory inspections** + **Assist with staffing and scheduling planning** for research activities **Qualifications** + **Bachelor’s degree** required; or **High School Diploma** with equivalent experience + **3 years of relevant clinical or medical experience** (e.g., medical assistant, nurse assistant, lab technician) + _Availability to work based in Rosario - Argentina_ + _Availability to work part-time (24 hours per week)_ + _Availability to work in a fixed term contract (6 months)_ + Working knowledge of **clinical trials** and **Good Clinical Practice (GCP)** + Strong understanding of **protocols, SOPs, consent forms, and study schedules** + Proficiency in **clinical procedures** (e.g., IV catheter insertion, spirometry) + Strong skills in **MS Windows and Office** (Access, Outlook, Word) + Excellent **interpersonal communication** abilities + High **attention to detail** + Ability to build and maintain **effective working relationships** with teams and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled