Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Adelaide or Brisbane
Core
Senior Clinical Research Associate managing and monitoring 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 Research
Required skills
Clinical site monitoring, regulatory compliance, data integrity verification, source document review, feasibility assessment, budget negotiation, vendor coordination, mentorship
Preferred skills
Advanced site management, drug development process knowledge
Technologies
Case Report Forms (CRFs), clinical trial management systems
Responsibilities
Monitor and manage clinical study sites (initiation, routine visits, closeout), review source documents and verify data integrity, prepare monitoring reports, coordinate with vendors and internal teams, support feasibility assessments and regulatory submissions, mentor junior team members
Seniority
Senior, hands-on IC
