On-Site Clinical Research Coordinator - Part-Time (24h)

IQVIA Inc; Thomasville (GA); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA Inc. is seeking a part-time Clinical Research Coordinator for an on-site role in Thomasville, GA.

The position supports clinical studies under the supervision of a principal investigator, performing procedures, patient recruitment, data collection, and compliance with GCP guidelines. The ideal candidate has a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with proficiency in EDC systems and strong attention to detail.

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

Attention to detail

Communication skills

GCP knowledge

Clinical data entry

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA Inc. is seeking a part-time Clinical Research Coordinator for an on-site role in Thomasville, GA.

The position supports clinical studies under the supervision of a principal investigator, performing procedures, patient recruitment, data collection, and compliance with GCP guidelines. The ideal candidate has a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with proficiency in EDC systems and strong attention to detail.