Tech Stack
Google Cloud Platform
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 (highly preferred)
- Minimum of 2 years of experience as a Clinical Research Associate (on site monitoring experience required)
- 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
- Competitive salary
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings
- Global Employee Assistance Programme (TELUS Health) with 24-hour access to over 80,000 independent specialised professionals
- Life assurance
- Flexible country-specific optional benefits (childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial processesprotocol compliancedata integritydata reviewquery resolutionstudy documentation preparationclinical study reportsICH-GCP guidelines
Soft skills
organizational skillscommunication skillsattention to detailindependent workcollaborative workability to work in fast-paced environment