Clinical Research Associate Jobs in Australia

Clinical Operations team at Parexel conducts clinical trials to improve global health. The Clinical Research Associate I, II monitors study sites, ensures protocol compliance, manages data quality, and supports investigators through on‑site and remote visits.

Clinical Research team at Covance conducts pivotal clinical studies to advance therapeutic development. The Senior Clinical Research Associate I oversees site monitoring and management, leads project coordination, ensures regulatory compliance, and mentors junior staff.

Thermo Fisher Scientific seeks a Senior Clinical Research Associate (Level I) to perform and coordinate clinical monitoring and site management across global trials. Day-to-day duties include risk-based site monitoring, data verification, regulatory compliance, documentation, and collaboration with investigative sites and sponsors.

As a Clinical Research Associate I (FSP) within Thermo Fisher Scientific, you will perform and coordinate clinical monitoring and site management to support global clinical trials. Day-to-day, you will conduct remote and on-site visits, apply risk-based monitoring with root cause analysis, review data and investigational product, document findings, and ensure compliance with ICH-GCP, protocols, and SOPs.

Senior Clinical Research Associate responsible for monitoring clinical trial sites, ensuring compliance with GCP and ICH guidelines, managing recruitment and enrollment, maintaining documentation, and coordinating with study teams to resolve issues and support project execution.

Thermo Fisher Scientific Clinical Research team advances global health by overseeing clinical trials across 100+ countries. The Senior Clinical Research Associate I conducts remote and on‑site monitoring, ensures protocol compliance, manages documentation, and drives risk‑based monitoring to maintain data integrity.

Clinical Monitoring, Site Management and SSU team at Premier Research ensures biotech, medtech and specialty pharma studies meet data integrity and patient safety standards. The Clinical Research Associate II delivers timely monitoring reports, conducts on‑site qualification and close‑out visits, and maintains the Trial Master File per ICH/GCP guidelines.

Join Covance as a Clinical Research Associate II in Sydney or Brisbane. Oversee site management, monitoring, and compliance for clinical trials, ensuring GCP adherence, data integrity, and audit readiness.

Novotech seeks a Clinical Research Associate to support Early Clinical Development and Phase I-III studies across Australia. The role involves independently monitoring clinical sites, ensuring trial safety and data integrity, and building partnerships with investigators and sponsors.

Perform site monitoring, manage recruitment, ensure GCP/ICH compliance, maintain TMF/ISF, generate reports, collaborate with study team, support financial management.

Thermo Fisher Scientific team enabling global health, safety and environmental impact. As a Senior Clinical Research Associate you will monitor investigator sites using risk‑based approaches, ensure data accuracy through source data verification, conduct root‑cause analysis, and mentor junior monitors while coordinating with clinical teams.

As a Clinical Research Associate II (Level II) within Thermo Fisher Scientific's PPD clinical operations team, you will perform and coordinate clinical monitoring and site management across global trials. Day-to-day, you will conduct remote or on-site monitoring visits, apply risk-based monitoring with root cause analysis, review data and investigational product, document findings, escalate issues, and support site initiation, close-out, and investigator meetings.

Fortrea is seeking a Clinical Research Associate II to manage and monitor clinical trials across Australia, ensuring regulatory compliance and fostering strong relationships with investigative sites. Day-to-day duties include conducting site monitoring visits, verifying source data, safeguarding subject protection, and maintaining audit readiness.

Thermo Fisher Scientific Clinical Operations team enables global health impact through rigorous clinical trial execution. The Senior Clinical Research Associate monitors investigator sites, ensures data accuracy, conducts risk‑based assessments, and mentors junior monitors while coordinating with clients and project teams.

Novotech is seeking a Senior Clinical Research Associate (FSP) to support Early Clinical Development and Phase I-III studies across Australia. In this role, you will independently manage and monitor assigned clinical trial sites, build partnerships with investigators and site personnel, drive site performance and patient recruitment, and protect participant safety and data integrity.

As a Clinical Research Associate (Level II) within the PPD project team, you will perform and coordinate all aspects of the clinical monitoring and site management process for pharmaceutical and biotech clients. You will conduct remote or on-site visits to assess protocol and regulatory compliance, manage procedures from sponsors such as FSO, FSP, and Government, and ensure trials follow the approved protocol, ICH-GCP guidelines, and SOPs.

Clinical Research Team at Covance conducts clinical trials to advance drug development. The Senior CRA leads site monitoring and management, ensures regulatory compliance, and mentors junior staff while coordinating travel and project tasks.

Thermo Fisher Scientific's PPD clinical research portfolio seeks a Senior Clinical Research Associate I (FSP) to perform and coordinate clinical monitoring and site management processes. The role conducts remote or on-site visits to assess protocol and regulatory compliance, manages documentation, applies risk-based monitoring with root cause analysis, and ensures audit readiness across clinical trials in 100+ countries.

Fortrea is seeking a Clinical Research Associate II (CRA2) in Melbourne to manage and monitor clinical trials, ensuring regulatory compliance and fostering relationships with investigative sites. The role involves conducting site monitoring visits, safeguarding data integrity, and acting as a Lead CRA when assigned within a hybrid work model.

TFS HealthScience, a global mid-size CRO, is building a network of Freelance Senior Clinical Research Associates (0.5 FTE) for an anticipated ophthalmology project within its Clinical Development Services (CDS) team. Based home in Sydney, Australia, the role involves initiation, on-site/remote monitoring, and close-out of study sites, providing unmasked CRA support including investigational product accountability, oversight of unblinded site activities, and protocol compliance monitoring.