Part-Time Clinical Research Coordinator – Savannah

Regulatory Jobs; Savannah (GA); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA in Savannah, GA is hiring a Clinical Research Coordinator (CRC) to support clinical studies under Principal Investigator supervision. This on-site role involves hands-on procedures, study coordination, and ensuring regulatory compliance and participant safety.

The CRC will perform ECGs, sample collection, vital signs, data entry into CRFs, and contribute to study material preparation, equipment setup, and daily trial activities.

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.

Skills

GCP knowledge

Clinical research

Data quality

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

IQVIA in Savannah, GA is hiring a Clinical Research Coordinator (CRC) to support clinical studies under Principal Investigator supervision. This on-site role involves hands-on procedures, study coordination, and ensuring regulatory compliance and participant safety.

The CRC will perform ECGs, sample collection, vital signs, data entry into CRFs, and contribute to study material preparation, equipment setup, and daily trial activities.