Clinical Research Assistant – Onsite

IQVIA Argentina; Kansas City (MO); On-site; USD 71,635,000 - 111,751,000; Part time

Job summary

IQVIA Site Research Assistant in Kansas City, MO is an onsite, part-time role supporting clinical studies under supervision of a principal investigator. You will perform hands-on clinical procedures, data entry in EDC, and ensure regulatory binder accuracy.

The ideal candidate has an Associate degree (or equivalent) and 1+ years in clinical research, with strong communication and detail orientation. Work closely with investigators and study teams in a dynamic environment.

Qualifications

• Associate degree preferred or equivalent combination of education and relevant experience.
• 1+ years of experience in a clinical research environment preferred.
• Strong working knowledge of clinical trials, GCP, and protocol-specific procedures.
• Proficiency with EDC systems, data entry accuracy, and query management.
• Experience with visit scheduling, regulatory documentation, and binder maintenance.

Responsibilities

• Perform accurate EDC data entry, manage queries, and ensure timely resolution.
• Maintain and update the regulatory binder in compliance with documentation and audit standards.
• Coordinate and schedule subject visits, procedures, and follow-up activities.
• Build effective working relationships with investigators, clinical staff, and study team members.
• Support subject screening, recruitment, and enrollment activities.
• Assist with patient scheduling and collection of medical history.
• Coordinate lab procedures and follow-up care in alignment with study protocols.
• Ensure strict adherence to IRB-approved protocols, including assistance with informed consent processes.
• Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.
• Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.

Skills

EDC data entry

Query management

Attention to detail

Communication

Education

Associate degree

Tools

EDC systems

Job description

IQVIA Site Research Assistant in Kansas City, MO is an onsite, part-time role supporting clinical studies under supervision of a principal investigator. You will perform hands-on clinical procedures, data entry in EDC, and ensure regulatory binder accuracy.

The ideal candidate has an Associate degree (or equivalent) and 1+ years in clinical research, with strong communication and detail orientation. Work closely with investigators and study teams in a dynamic environment.