# Clinical Research Associate

**Company**: IQVIA
**Location**: Reading, Berkshire
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Senior-Clinical-Research-Associate_R1510425?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ba4b9ffa-6bc

## Description

Join IQVIA on its mission to drive healthcare forward as a Clinical Research Associate in the UK.

IQVIA, a leading global provider of clinical research services, commercial insights, and healthcare intelligence, is seeking experienced Clinical Research Associates.

**Why IQVIA?**

- Recognized as #1 in its category on the 2026 Fortune World's Most Admired Companies list for the fifth consecutive year

- Genuine career development opportunities

- Work on cutting-edge medicines at the forefront of new medicines development

- Access to significant data pools for better site selection and recruitment

**Responsibilities**

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

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

- Administer protocol and related study training to assigned sites

- Evaluate the quality and integrity of study site practices

- Manage the progress of assigned studies

- Ensure site documents are available for filing in the Trial Master File

- Create and maintain documentation regarding site management and monitoring visit findings

- Collaborate with study team members for project execution support

**Requirements**

- Minimum of 18 months of independent on-site monitoring

- Experience managing multiple clinical trial protocols across diverse investigative sites

- In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Life science degree educated or equivalent industry experience

- Flexibility to travel to sites

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

*Please note - this role is not eligible for UK visa sponsorship*

## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- clinical trial management
- site monitoring

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Senior-Clinical-Research-Associate_R1510425?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)