Clinical Research Coordinator – Onsite, 24 hrs/week

IQVIA; Jefferson City (MO); On-site; USD 4,822,000 - 5,786,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Jefferson City, MO. The role involves hands-on clinical procedures, study coordination, and ensuring GCP-compliant operations with a strong focus on patient safety.

The ideal candidate will have a Bachelor’s degree (or equivalent), 1+ year of clinical research experience, and familiarity with EDC systems and data quality processes. This is a 24-hour/week on-site position.

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 GCP guidelines.
• Support study conducts by preparing materials, setting up equipment, and planning logistics.
• 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 line with Health and Safety policies.

Skills

Attention to detail

Data entry accuracy

GCP principles

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Query management

Job description

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Jefferson City, MO. The role involves hands-on clinical procedures, study coordination, and ensuring GCP-compliant operations with a strong focus on patient safety.

The ideal candidate will have a Bachelor’s degree (or equivalent), 1+ year of clinical research experience, and familiarity with EDC systems and data quality processes. This is a 24-hour/week on-site position.