Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Perth, Adelaide or Brisbane
Core
Manage and monitor clinical study sites to ensure patient safety, data integrity, and regulatory compliance in pharmaceutical trials.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data and regulatory compliance
Domain
Life sciences / Clinical trials
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Site initiation and closeout management, Source document review, Case Report Form (CRF) verification, Monitoring plan development, Vendor coordination, Feasibility assessment, Budget negotiation, Regulatory submission support, Junior team mentorship
Preferred skills
Advanced site management, Drug development process knowledge
Technologies
Computer applications and clinical systems
Responsibilities
Monitor and manage clinical study sites, Ensure patient safety and informed consent compliance, Review source documents and verify data integrity, Prepare monitoring reports and maintain study files, Coordinate with vendors and internal teams, Support feasibility assessments and regulatory submissions, Mentor and train junior team members
Seniority
Senior, hands-on IC