Clinical Research Coordinator (Rosario)

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 protocolrequired 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 studyrelated 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

• Bachelors 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

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.