# Freelance Clinical Research Associate

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Freelance-CRA----Czech-Republic_R1569955?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_9cdf1ac3-63e

## Description

Join IQVIA Biotech as a Freelance Clinical Research Associate supporting two Phase III Oncology clinical trials. You'll lead site visits, monitor compliance, and ensure high-quality data,all while working with a team.

**Your Role**

- Conduct site evaluations, initiations, monitoring & close-outs

- Ensure GCP compliance and data integrity

- Collaborate with investigators and internal teams

- Review protocols, study manuals, and eCRFs

- Support site staff with training and issue resolution

- Track investigational product inventory and documentation

- Attend investigator meetings and study-related events

- Contribute to audit readiness and inspection support

**Your Profile:**

- 2+ years CRA including site monitoring experience

- Oncology/Hematology experience

- Strong knowledge of clinical trial processes & GCP

- Excellent communication & organisational skills

- Ability to work independently and manage priorities

- Fluent in Czech and English

If you're ready to make an impact in clinical research, apply today!

## Skills

### Required
- Clinical Research
- Oncology
- Hematology
- GCP
- Czech
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Freelance-CRA----Czech-Republic_R1569955?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)