# Freelance CRA

**Company**: IQVIA
**Experience**: senior
**Job type**: contract
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Barcelona-Spain/Freelance-CRA----Spain_R1570734?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e3eb1a0c-bd7

## Description

We are currently looking for two experienced CRAs, each supporting approximately 0.5 FTE (18 hours/week), with the possibility of combining assignments depending on availability and project needs. The role focuses primarily on monitoring activities across sites throughout Spain.

Responsibilities:

- Perform Interim Monitoring Visits (IMVs) at clinical trial sites

- Ensure protocol adherence and ICH-GCP compliance

- Verify source documents and study data

- Support investigators and site personnel

- Identify and follow up on site issues and action plans

- Collaborate with project teams to ensure successful study delivery

Requirements:

- Minimum 2 years of CRA monitoring experience

- Previous Phase III clinical trial experience

- Strong knowledge of ICH-GCP and clinical trial processes

- Ability to work independently

- Excellent communication and organizational skills

- Fluent Spanish and English

- Willingness to travel within Spain

## Skills

### Required
- ICH-GCP
- clinical trial processes
- Spanish
- English
- CRA monitoring

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Barcelona-Spain/Freelance-CRA----Spain_R1570734?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)