# Research Assistant

**Company**: IQVIA
**Location**: Kansas City, MO
**Work arrangement**: onsite
**Salary**: $25.00-$39.00 per hour
**Category**: Research
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kansas-City-MO/Site-Research-Assistant---Kansas-City--MO_R1561497?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_790bbb5a-944

## Description

We are seeking a Research Assistant (RA) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.

**Key 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.

**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.

- Excellent attention to detail, time management, and task prioritization.

- Strong communication, interpersonal, and relationship-building skills.

The potential base pay range for this role is $25.00-$39.00 per hour.

## Skills

### Required
- EDC systems
- data entry
- clinical trials
- GCP
- protocol-specific procedures
- regulatory documentation
- Good Clinical Practice

### Nice to have
- associate degree
- 1+ years of experience in clinical research environment
- visit scheduling
- binder maintenance
- relationship-building skills

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kansas-City-MO/Site-Research-Assistant---Kansas-City--MO_R1561497?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)