About this role
About the Role ICON plc is seeking a Clinical Research Associate to support monitoring and oversight of clinical trials in Guangzhou. You will contribute to trial design and analysis, interpret complex medical data, and help advance innovative treatments and therapies. The role requires collaboration with investigative sites and travel (approximately 60%). What You'll Do
- 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 resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports. What We're Looking For
- 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 organizational 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%). Compensation & Benefits
- Competitive salary and a range of benefits designed to support well-being and work-life balance.
- Various annual leave entitlements.
- Health insurance offerings.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme (LifeWorks) with 24-hour access to a global network of professionals.
- Life assurance.
- Flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, gym memberships discounts, subsidized travel passes, health assessments).
- Visit ICON careers site to read more about the benefits ICON offers.