Site Research Assistant - Kansas City, Mo

IQVIA UK

Kansas City, MO, US
Base: $25.00-$39.00 ph; bonus/equity: not specifie...
Onsite
Edc data entry and query resolution
Patient chart review and prescreening
Gcp and irb regulatory compliance
The Site Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB requirements, and all applicable regulations

Job Summary

  • The Site Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB requirements, and all applicable regulations.
  • Key responsibilities include performing EDC data entry, resolving queries accurately, reviewing patient charts, and assisting with participant recruitment and enrollment.
  • IQVIA is a global leader dedicated to driving healthcare forward by partnering with pharmaceutical and biotechnology companies to improve patient outcomes.

Matching Summary

The Site Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB requirements, and all applicable regulations.

Salary

Base: $25.00-$39.00 per hour; Bonus/Equity: Not specified; Benefits: Range of health and welfare benefits offered

Skills & Requirements

Must-have

  • EDC data entry and query resolution
  • Patient chart review and prescreening
  • GCP and IRB regulatory compliance
  • Participant visit scheduling and coordination
  • Informed consent process support

Nice-to-have

  • Experience in cardiovascular studies
  • Strong attention to detail in fast-paced environment
  • Effective communication with investigators and staff

Key Requirements

  • Minimum of an associate's degree or equivalent education
  • At least 1 year of experience in a clinical research setting
  • Working knowledge of clinical trials, GCP, and study-specific procedures
  • Ability to perform required clinical procedures and understand medical terminology

Work Rights

Not specified

Tailored Resume

Cover Letter