Clinical Research Associate (Home-based, Brisbane)
Core
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements.
Role type
Junior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biopharma and medical device clients
Domain
Clinical Research / Biopharmaceuticals
Deliverable
client delivery
Required skills
Clinical monitoring, regulatory document review, medical record verification, adverse event reporting, investigator qualification verification, site compliance assessment
Preferred skills
Study coordinator experience, clinical research coordinator experience, knowledge of clinical monitoring practices
Technologies
GCP, SOPs, Case Report Forms (CRF)
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation; Verify adverse event reporting; Assess patient recruitment and retention success
Seniority
Junior, entry-level with training
