Senior Clinical Research Associate / Clinical Research Associate II
ICON plc
full-time
Posted on:
Location Type: Hybrid
Location: Melbourne • Australia
Visit company websiteExplore more
Job Level
Tech Stack
About the role
- 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
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 1.5 years of experience as a Clinical Research Associate, with strong Oncology monitoring experience.
- 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.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Benefits
- 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.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial processesprotocol compliancedata integritydata reviewquery resolutionstudy documentation preparationclinical study reportsOncology monitoringICH-GCP guidelines
Soft Skills
organizational skillscommunication skillsattention to detailindependent workcollaborative workability to work in fast-paced environment
Certifications
Bachelor's degree in scientific fieldBachelor's degree in healthcare-related field