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

IQVIA; Parsippany-Troy Hills (NJ); Presencial; USD 100.289.000 - 120.402.000; Jornada completa

Descripción de la vacante

IQVIA LLC is seeking a Clinical Research Coordinator to join our on-site team in Boulder, CO. You will perform clinical procedures, recruit and screen patients, and ensure data quality under supervision of a principal investigator.

The role requires a Bachelor’s degree (or equivalent) and 1+ years in clinical research, with strong knowledge of GCP and familiarity with EDC systems. On-site position with a focus on patient safety and compliance.

Formación

• 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.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsabilidades

• 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 conducts 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.

Conocimientos

Clinical research

GCP principles

Medical terminology

Attention to detail

Communication

Educación

Bachelor’s degree or equivalent

Herramientas

EDC systems

Descripción del empleo

IQVIA LLC is seeking a Clinical Research Coordinator to join our on-site team in Boulder, CO. You will perform clinical procedures, recruit and screen patients, and ensure data quality under supervision of a principal investigator.

The role requires a Bachelor’s degree (or equivalent) and 1+ years in clinical research, with strong knowledge of GCP and familiarity with EDC systems. On-site position with a focus on patient safety and compliance.