Part-Time Clinical Research Coordinator (On-Site)

IQVIA; El Paso (TX); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA in El Paso, TX is seeking a part-time Clinical Research Coordinator to join our onsite team for 24 hours per week. You will oversee clinical procedures, patient recruitment, data collection, and ensure GCP-compliant study conduct under supervision of a principal investigator.

The role requires a Bachelor’s degree or equivalent, 1+ year in clinical research, and proficiency with EDC systems. On-site setting with emphasis on accuracy and patient safety.

Qualifications

• Bachelor's degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, 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

GCP principles

Data entry accuracy

Attention to detail

Communication

Education

Bachelor’s degree or equivalent

Job description

IQVIA in El Paso, TX is seeking a part-time Clinical Research Coordinator to join our onsite team for 24 hours per week. You will oversee clinical procedures, patient recruitment, data collection, and ensure GCP-compliant study conduct under supervision of a principal investigator.

The role requires a Bachelor’s degree or equivalent, 1+ year in clinical research, and proficiency with EDC systems. On-site setting with emphasis on accuracy and patient safety.