Onsite Clinical Research Coordinator - 24h/Part-Time

iqvia; Missouri; On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in Jefferson City, Missouri. This on-site role operates at 24 hours per week and involves direct patient interactions, study coordination, and data collection under the supervision of the principal investigator.

Responsibilities include performing ECGs, sample collection, vital signs, and ensuring adherence to GCP. A bachelor’s degree or equivalent plus 1+ year clinical research experience are preferred; EDC systems proficiency is expected.

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.
• 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

Communication skills

Education

Bachelor’s degree preferred or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator in Jefferson City, Missouri. This on-site role operates at 24 hours per week and involves direct patient interactions, study coordination, and data collection under the supervision of the principal investigator.

Responsibilities include performing ECGs, sample collection, vital signs, and ensuring adherence to GCP. A bachelor’s degree or equivalent plus 1+ year clinical research experience are preferred; EDC systems proficiency is expected.