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.
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
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)
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.