On-Site Clinical Research Coordinator — Hands-On Trials

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

Job summary

IQVIA is seeking a Clinical Research Coordinator (CRC) to join our on-site team in Frisco, TX, supporting clinical studies under a principal investigator. This role involves hands-on procedures, patient recruitment, and ensuring compliance with GCP and study protocols.

The CRC will perform ECGs, vital signs, data entry into CRFs, coordinate study activities, and maintain documentation. A bachelor's degree and 1+ year of clinical research experience are preferred; familiarity with EDC systems is

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 conduct 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

Clinical trials knowledge

GCP principles

Data entry accuracy

Attention to detail

EDC systems

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator (CRC) to join our on-site team in Frisco, TX, supporting clinical studies under a principal investigator. This role involves hands-on procedures, patient recruitment, and ensuring compliance with GCP and study protocols.

The CRC will perform ECGs, vital signs, data entry into CRFs, coordinate study activities, and maintain documentation. A bachelor's degree and 1+ year of clinical research experience are preferred; familiarity with EDC systems is