On-Site Clinical Research Coordinator – Part-Time (Boulder)

IQVIA Argentina; Boulder (CO); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA in Boulder, CO is seeking a Clinical Research Coordinator to assist with hands-on clinical procedures under a principal investigator. This on-site position is 24 hours per week and focuses on data collection, patient safety, and adherence to GCP.

Key tasks include ECG, sample collection, vital signs, coordinating studies, preparing materials, recruiting and orienting patients, and entering data into CRFs while ensuring data quality and regulatory compliance.

Qualifications

• Bachelor’s degree or equivalent education/experience.
• Minimum 1+ year of relevant clinical research experience.
• Knowledge of trials, GCP, and medical terminology.
• Proficiency with EDC systems and data queries.

Responsibilities

• Perform ECG, sample collection, and vital signs.
• Coordinate studies and ensure protocol/GCP compliance.
• Prepare materials, set up equipment, plan logistics.
• Recruit, screen, and orient patients safely.
• Record data in CRFs accurately.
• Collaborate with investigators and monitors on data quality.

Skills

Clinical research

GCP principles

Attention to detail

Communication

Data entry accuracy

Patient safety

Education

Bachelor's degree or equivalent education/experience

Tools

EDC systems

Job description

IQVIA in Boulder, CO is seeking a Clinical Research Coordinator to assist with hands-on clinical procedures under a principal investigator. This on-site position is 24 hours per week and focuses on data collection, patient safety, and adherence to GCP.

Key tasks include ECG, sample collection, vital signs, coordinating studies, preparing materials, recruiting and orienting patients, and entering data into CRFs while ensuring data quality and regulatory compliance.