On-Site Clinical Research Coordinator — 24h/Week

IQVIA; Union (SC); On-site; USD 31,000 - 44,000; Part time

Job summary

IQVIA seeks a Clinical Research Coordinator to join our on-site team in Union, SC. This 24-hour/week role supports clinical studies under the supervision of a principal investigator, performing procedures and coordinating study activities.

The CRC ensures GCP compliance, accurate data collection, and patient safety, while liaising with investigators, monitors, and study staff to keep trials running smoothly in a collaborative environment.

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

ECG

Vital signs

Data collection

GCP awareness

Attention to detail

Communication skills

Education

Bachelor’s degree

Tools

EDC systems

Job description

IQVIA seeks a Clinical Research Coordinator to join our on-site team in Union, SC. This 24-hour/week role supports clinical studies under the supervision of a principal investigator, performing procedures and coordinating study activities.

The CRC ensures GCP compliance, accurate data collection, and patient safety, while liaising with investigators, monitors, and study staff to keep trials running smoothly in a collaborative environment.