Part-Time Clinical Research Coordinator – On-Site GA

IQVIA Inc; Tallahassee (FL); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Thomasville, GA, supporting clinical studies under a principal investigator. The role involves hands-on procedures, patient coordination, and ensuring compliance with GCP.

Candidates should have a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with proficiency in EDC systems and data entry. This position is not sponsorship eligible.

Qualifications

• Bachelor’s degree 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.
• 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 research

Data entry

GCP knowledge

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Thomasville, GA, supporting clinical studies under a principal investigator. The role involves hands-on procedures, patient coordination, and ensuring compliance with GCP.

Candidates should have a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with proficiency in EDC systems and data entry. This position is not sponsorship eligible.