Clinical Research Coordinator — On-Site, 24hrs/week

Regulatory Jobs; Thomasville (GA); Vor Ort; USD 48.000 - 58.000; Teilzeit

Zusammenfassung

IQVIA is seeking a Clinical Research Coordinator to support studies in Thomasville, GA. This on-site role offers 24 hours per week and requires hands-on procedures, patient screening, data entry, and adherence to GCP.

Candidates should have a Bachelor's degree or equivalent and at least 1 year in clinical research; familiarity with ECG, vital signs, and EDC systems is preferred. Note: sponsorship is not available.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

GCP knowledge

Medical terminology

Data entry accuracy

EDC systems

Clinical data collection

Patient safety

Ausbildung

Bachelor’s degree or equivalent

Tools

CRF data entry tools

Jobbeschreibung

IQVIA is seeking a Clinical Research Coordinator to support studies in Thomasville, GA. This on-site role offers 24 hours per week and requires hands-on procedures, patient screening, data entry, and adherence to GCP.

Candidates should have a Bachelor's degree or equivalent and at least 1 year in clinical research; familiarity with ECG, vital signs, and EDC systems is preferred. Note: sponsorship is not available.