Part-Time Clinical Research Coordinator – On-Site

Regulatory Jobs; Jefferson City (MO); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA in Jefferson City, MO is seeking a Clinical Research Coordinator to join our team on-site. This role involves performing clinical procedures, coordinating studies, and ensuring compliance with GCP guidelines under the supervision of a principal investigator.

Responsibilities include ECGs, sample collection, patient recruitment and data entry into CRFs, plus collaboration with investigators and monitors to maintain data quality and patient safety.

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 ECG, sample collection, and vital signs.
• Coordinate clinical research studies and ensure GCP compliance.
• Prepare study materials, set up equipment, and plan logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well‑being.
• Collect and 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 per Health and Safety policies.

Skills

Attention to detail

Data entry accuracy

Communication skills

Team collaboration

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA in Jefferson City, MO is seeking a Clinical Research Coordinator to join our team on-site. This role involves performing clinical procedures, coordinating studies, and ensuring compliance with GCP guidelines under the supervision of a principal investigator.

Responsibilities include ECGs, sample collection, patient recruitment and data entry into CRFs, plus collaboration with investigators and monitors to maintain data quality and patient safety.