On-Site Clinical Research Coordinator — ECG & Data Capture

IQVIA Argentina; El Paso (TX); On-site; USD 100,289,000 - 120,347,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in El Paso, TX to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient recruitment, and ensuring adherence to GCP and study protocols.

You will perform ECGs and vital signs, manage data entry in CRFs, coordinate visits, and collaborate with monitors to ensure data quality and participant safety in accordance with health and safety policies.

Qualifications

• Bachelor's degree or equivalent combination of education and relevant experience.
• Minimum 1+ year of experience in clinical research.
• Working knowledge of clinical trials, GCP, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well‑being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

EDC systems

data entry accuracy

query management

attention to detail

GCP principles

Education

Bachelor's degree preferred

Job description

IQVIA is seeking a Clinical Research Coordinator in El Paso, TX to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient recruitment, and ensuring adherence to GCP and study protocols.

You will perform ECGs and vital signs, manage data entry in CRFs, coordinate visits, and collaborate with monitors to ensure data quality and participant safety in accordance with health and safety policies.