On-Site Clinical Research Coordinator: Elevate Care

IQVIA LLC; Parsippany-Troy Hills (NJ); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in El Paso, TX. This on-site role supports clinical research studies under the supervision of a principal investigator.

You will perform hands-on procedures, assist with study materials, and help ensure patient safety and protocol compliance. The ideal candidate has a bachelor’s degree or equivalent and at least 1 year of clinical research experience, knowledge of GCP, and experience with EDC systems.

Qualifications

• Bachelor’s degree or equivalent in a relevant field.
• Minimum 1+ year of clinical research experience.
• Working knowledge of clinical trials, GCP, and medical terminology.
• Strong attention to detail and relationship-building abilities.
• Proficiency with EDC systems and data-query management.

Responsibilities

• Perform clinical procedures including ECG, sample collection and vital signs.
• Coordinate studies and ensure compliance with protocols and GCP.
• Prepare study materials, set up equipment, and plan logistics.
• Recruit, screen and orient patients for the study.
• Record data accurately in case report forms (CRFs).
• Collaborate with investigators and monitors to resolve queries.

Skills

Clinical research

GCP knowledge

Medical terminology

EDC systems

Data entry

Query management

Attention to detail

Education

Bachelor’s degree or equivalent

Job description

IQVIA is seeking a Clinical Research Coordinator in El Paso, TX. This on-site role supports clinical research studies under the supervision of a principal investigator.

You will perform hands-on procedures, assist with study materials, and help ensure patient safety and protocol compliance. The ideal candidate has a bachelor’s degree or equivalent and at least 1 year of clinical research experience, knowledge of GCP, and experience with EDC systems.