# Clinical Research Associate

**Company**: ICON Strategic Solutions
**Location**: Chengdu, China
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Chengdu/CRA-II_JR163134?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-research-associate-5ac073f8-b56/

## Description

As a Clinical Research Associate (CRA II) at ICON Strategic Solutions in Chengdu, China, or Nanjing, China, you will play a crucial role in designing and analysing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

**Key Responsibilities:**

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

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

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

- Perform data review and resolve queries to maintain high-quality clinical data.

- Contribute to preparing and reviewing 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 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.

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## Skills

### Required
- clinical trial monitoring
- ICH-GCP guidelines
- data analysis
- communication skills
- organisational skills

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