Part-Time Clinical Research Coordinator: Hands-On Trials

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

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our Boulder, CO team. This on-site, part-time role (24 hours/week) supports clinical studies under the supervision of a principal investigator, performing clinical procedures, coordinating logistics, and maintaining high standards of patient safety and data integrity.

The successful candidate will have a Bachelor’s degree (or equivalent), at least 1 year in clinical research, knowledge of GCP, and proficiency with EDC systems.

Qualifications

• Bachelor’s degree or equivalent required.
• Minimum 1+ years of clinical research experience.
• Working knowledge of GCP, clinical trials terminology.
• Detail-oriented with strong teamwork skills.
• Proficiency with EDC systems and data entry accuracy.

Responsibilities

• Perform clinical procedures (ECG, sample collection, vitals).
• Coordinate studies and ensure protocol and GCP compliance.
• Prepare study materials, set up equipment, and plan logistics.
• Recruit, screen and orient patients ensuring safety.
• Record data accurately in CRFs and support data quality.

Skills

EDC systems

GCP principles

Clinical research

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to join our Boulder, CO team. This on-site, part-time role (24 hours/week) supports clinical studies under the supervision of a principal investigator, performing clinical procedures, coordinating logistics, and maintaining high standards of patient safety and data integrity.

The successful candidate will have a Bachelor’s degree (or equivalent), at least 1 year in clinical research, knowledge of GCP, and proficiency with EDC systems.