Onsite Clinical Research Coordinator - ECG & Study Ops

IQVIA LLC; Boulder (CO); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA LLC in Boulder, CO is seeking a Clinical Research Coordinator to support studies under a principal investigator. The on-site role focuses on hands-on procedures, patient safety, and GCP compliance.

Responsibilities include performing ECGs, vital signs, sample collection, data entry into CRFs, and coordinating study logistics. A Bachelor’s degree or equivalent and 1+ year of experience are preferred; proficiency with EDC systems is desired.

Qualifications

• 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.

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 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.

Skills

Attention to detail

Communication

Team collaboration

Clinical terminology

Education

Bachelor's degree

Tools

EDC systems

Job description

IQVIA LLC in Boulder, CO is seeking a Clinical Research Coordinator to support studies under a principal investigator. The on-site role focuses on hands-on procedures, patient safety, and GCP compliance.

Responsibilities include performing ECGs, vital signs, sample collection, data entry into CRFs, and coordinating study logistics. A Bachelor’s degree or equivalent and 1+ year of experience are preferred; proficiency with EDC systems is desired.