On-Site Clinical Research Coordinator | 24h/Week

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

Job summary

IQVIA in Boulder, CO is seeking a part-time Clinical Research Coordinator to support ongoing studies under the supervision of a principal investigator. This on-site role requires hands-on procedures, patient recruitment, data collection, and strict adherence to GCP guidelines.

The ideal candidate has a bachelor’s degree (or equivalent) and at least one year of clinical research experience, strong attention to detail, and proficiency with EDC systems.

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

Relationship building

Communication skills

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA in Boulder, CO is seeking a part-time Clinical Research Coordinator to support ongoing studies under the supervision of a principal investigator. This on-site role requires hands-on procedures, patient recruitment, data collection, and strict adherence to GCP guidelines.

The ideal candidate has a bachelor’s degree (or equivalent) and at least one year of clinical research experience, strong attention to detail, and proficiency with EDC systems.