Clinical Research Associate – CRA, Level Depending on Experience
CTI Clinical Trial and Consulting Services
full-time
Posted on:
Location Type: Hybrid
Location: Queensland • 🇦🇺 Australia
Visit company websiteJob Level
JuniorMid-Level
About the role
- Serve as main CTI contact for assigned study sites
- Conduct site visits and complete site visit deliverables
- Assist with or oversee study start-up activities
- Collect, review and track essential/regulatory documents
- Participate in training and meetings
- Create and implement subject enrollment strategies
- Ensure proper storage and accountability of trial-related materials
- Perform remote monitoring and related activities
- Manage ISF and TMF for assigned study sites
- Identify and anticipate site issues and implement corrective actions
- Liaise with Clinical Data Management for data cleaning activities
Requirements
- At least 3 years of clinical trial monitoring experience or equivalent experience
- Fluent in English
- Bachelor's Degree or higher in allied health field or RN with Associate's Degree, or 3-year Nursing Diploma with clinical nursing experience
- Previous experience in conducting clinical research studies in hospital setting, pharmaceutical company or CRA
- Must be fully eligible to work in Australia
Benefits
- Generous health benefits
- Vacation packages
- Paid parental leave
- Hybrid work from home opportunities
- Structured mentoring program
- Leadership courses
- Ongoing education and training through tuition reimbursement
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial monitoringsite visit deliverablesstudy start-up activitiesregulatory document trackingsubject enrollment strategiesremote monitoringISF managementTMF managementdata cleaning
Soft skills
communicationproblem-solvingorganizational skillsleadershiptraining
Certifications
Bachelor's DegreeRN with Associate's Degree3-year Nursing Diploma