On-Site Clinical Research Coordinator (Thomasville, GA) 24h

IQVIA Inc; Parsippany-Troy Hills (NJ); In loco; USD 48.000 - 58.000; Tempo pieno

Descrizione del lavoro

IQVIA is a global leader in clinical research services, analytics, and technology solutions seeking a Clinical Research Coordinator to support studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient recruitment, data collection, and ensuring patient safety in a compliant environment.

Responsibilities include coordinating studies, preparing materials, and maintaining data quality.

Competenze

• 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.

Mansioni

• 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.

Conoscenze

Attention to detail

GCP knowledge

Clinical research experience

Data entry accuracy

Formazione

Bachelor’s degree preferred

Strumenti

EDC systems

Descrizione del lavoro

IQVIA is a global leader in clinical research services, analytics, and technology solutions seeking a Clinical Research Coordinator to support studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient recruitment, data collection, and ensuring patient safety in a compliant environment.

Responsibilities include coordinating studies, preparing materials, and maintaining data quality.