# Clinical Research Associate

**Company**: ICON Strategic Solutions
**Location**: Miami, FL
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR162721-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As a Clinical Research Associate (CRA II) at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This position is sponsor dedicated supporting our client monitoring cardio and obesity trials. The salary is not specified.

**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.

- Willingness to travel as required (approximately 60%).

**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 monitoring
- data analysis
- ICH-GCP guidelines
- communication skills
- organisational skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR162721-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)