# Clinical Research Associate

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Salary**: €34,300.00 - €63,100.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Milan-Italy/Experienced-Clinical-Research-Associate--IQVIA-Biotech---Home-based--Italy_R1575628?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_0cffce3a-ecb

## Description

We are seeking a Clinical Research Associate to perform monitoring and site management work, ensuring sites conduct studies and report data as required by study protocols, regulations, and sponsor requirements.

The successful candidate will have a University Bachelor's Degree and Master's Degree in a scientific discipline or healthcare, possess CRA Certification as required by Ministerial Decree dated 15.11.2011, and have experience in the pharma industry and/or clinical trials environment.

Key responsibilities include:

- Performing site monitoring visits in accordance with contracted scope of work and regulatory requirements

- Working with sites to adapt, drive, and track subject recruitment plans

- Administering protocol and related study training to assigned sites

- Evaluating the quality and integrity of study site practices

- Managing study progress by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution

- Ensuring site documents are available for filing in the Trial Master File (TMF) and verifying the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements

- Creating and maintaining documentation regarding site management, monitoring visit findings, and action plans

- Collaborating with study team members for project execution support

The potential base pay range for this role, when annualized, is €34,300.00 - €63,100.00.

## Skills

### Required
- CRA Certification
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- MS Office
- English language

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Milan-Italy/Experienced-Clinical-Research-Associate--IQVIA-Biotech---Home-based--Italy_R1575628?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)