# Clinical Research Associate II

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Shanghai/Clinical-Research-Associate-II_JR160122?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_b4fa5e7b-7c2

## Description

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

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

**What You Will Do:**

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:

- 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:**

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:

- 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**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- 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/China-Shanghai/Clinical-Research-Associate-II_JR160122?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)