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Clinical Research Associate
ICON plcCRA II at ICON conducting clinical trial monitoring and ensuring compliance while collaborating with site staff. Analyzing clinical data and contributing to innovative treatments and therapies.
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
- 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.
Requirements
What you’ll need- 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%)
Benefits
Comp & perks- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringsite qualificationdata reviewprotocol compliancedata integritypatient safetystudy documentation preparationclinical study reportsquery resolutionclinical trial processes
Soft Skills
organizational skillscommunication skillsattention to detailindependent workcollaborative workadaptabilityproblem-solvingtime managementinterpersonal skillsteamwork