Clinical Research Assistant — On‑Site (Part‑Time)

IQVIA LLC; Parsippany-Troy Hills (NJ); On-site; USD 34,000 - 54,000; Part time

Job summary

IQVIA seeks a part-time Research Assistant to support clinical studies under a Principal Investigator. On-site in Kansas City, MO, you will handle data entry in EDC, maintain regulatory binders, coordinate visits, and assist with enrollment while upholding GCP standards.

The role requires at least an Associate degree (or equivalent) and 1+ years in clinical research. Strong communication and meticulous attention to detail are essential.

Qualifications

• Associate degree or equivalent required.
• 1+ years experience in clinical research preferred.
• Strong knowledge of GCP and regulatory procedures.
• Proficiency with EDC systems and data entry accuracy.
• Experience with visit scheduling 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/research participant 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

Clinical research knowledge

Attention to detail

Time management

Communication skills

Education

Associate degree or equivalent

Tools

EDC systems

Job description

IQVIA seeks a part-time Research Assistant to support clinical studies under a Principal Investigator. On-site in Kansas City, MO, you will handle data entry in EDC, maintain regulatory binders, coordinate visits, and assist with enrollment while upholding GCP standards.

The role requires at least an Associate degree (or equivalent) and 1+ years in clinical research. Strong communication and meticulous attention to detail are essential.