About this role
About the Role ICON is seeking a Clinical Research Associate (CRA II) for Early Development Multi-Therapeutic roles in a regional hub. You will contribute to designing and monitoring clinical trials, interpreting complex medical data, and advancing innovative therapies in collaboration with investigators and site staff.
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 ICON offers a range of benefits including various annual leave entitlements, a range of health insurance offerings to suit you and your family’s needs, competitive retirement planning offerings, Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being, life assurance, flexible country-specific optional benefits including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. ICON is committed to inclusion & belonging and providing equal opportunity for all qualified applicants.