Part-Time Clinical Research Coordinator — On-Site in Boulder

IQVIA; Colorado; Presencial; USD 48 000 - 58 000; Tempo parcial

Resumo da oferta

IQVIA in Boulder, CO is seeking a Clinical Research Coordinator to support clinical studies under a principal investigator. This on-site role involves hands-on clinical procedures, data collection, and ensuring compliance with GCP guidelines.

The CRC will recruit and screen participants, manage case report forms, coordinate study activities, and maintain safety and quality across procedures, data entry, and query resolution, working closely with investigators and monitors.

Qualificações

• 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.

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.

Conhecimentos

GCP principles

Data entry accuracy

Attention to detail

Formação académica

Bachelor’s degree or equivalent

Ferramentas

EDC systems

Descrição da oferta de emprego

IQVIA in Boulder, CO is seeking a Clinical Research Coordinator to support clinical studies under a principal investigator. This on-site role involves hands-on clinical procedures, data collection, and ensuring compliance with GCP guidelines.

The CRC will recruit and screen participants, manage case report forms, coordinate study activities, and maintain safety and quality across procedures, data entry, and query resolution, working closely with investigators and monitors.