# Clinical Research Associate

**Company**: ICON
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Clinical-Research-Associate_JR141958?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ccd63ba1-e28

## Description

ICON is seeking a Clinical Research Associate II to join their team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

**Responsibilities**

- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

- Collaborating with investigators and site staff to facilitate smooth study conduct.

- Performing data review and resolution of queries to maintain high-quality clinical data.

- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

**Your Profile**

- Bachelor's degree in a scientific or healthcare-related field.

- Minimum of 2 years of experience as a Clinical Research Associate.

- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

- Strong organisational and communication skills, with attention to detail.

- Ability to work independently and collaboratively in a fast-paced environment.

- Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license.

**Rewards & Benefits**

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

## Skills

### Required
- clinical trial processes
- ICH-GCP guidelines
- organisational skills
- communication skills

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