# 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/Experienced-CRA---Single-Sponsor-Dedicated_R1524544?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_1b046d7e-63f

## Description

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

IQVIA, a recognised leader in clinical research services, is seeking experienced professionals to join its team.

**Responsibilities:**

- Conduct site monitoring visits, including selection, initiation, monitoring, and close-out visits, adhering to contracted scope of work and regulatory requirements such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Collaborate with sites to adapt, drive, and track subject recruitment plans, ensuring alignment with project needs and enhancing predictability

- Provide protocol and related study training to assigned sites, establishing regular communication channels to manage ongoing project expectations and issues

- Evaluate the quality and integrity of study site practices, ensuring compliance with the protocol and applicable regulations, and escalate quality issues as necessary

- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution

- Ensure site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained according to GCP and local regulatory requirements

- Create and maintain documentation regarding site management, monitoring visit findings, and action plans through regular visit reports, follow-up letters, and other required study documentation

- Collaborate with study team members to support project execution

**Requirements:**

- Minimum 6 months of experience in independent on-site monitoring

- Proven ability to manage 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 education or equivalent industry experience

- Flexibility to travel to sites

**What We Offer:**

- Opportunities for genuine career development within the organisation

- Chance to work on cutting-edge medicines at the forefront of new medicines development

- Access to significant data pools to enhance site selection, recruitment, and performance

**Note:** This role is not eligible for UK visa sponsorship.

## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH)
- Life science degree

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Experienced-CRA---Single-Sponsor-Dedicated_R1524544?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)