Clinical Research Associate Jobs in Australian Capital Territory, Australia

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.

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.

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.

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.

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.

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.

Premier Research is looking for a Senior Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics.

The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor.

Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics.

The Senior Clinical Research Associate I monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable regulations. Builds, manages and supports strong site relationships while serving as liaison between the Sponsor and assigned sites.

As a CRA, you will play a critical role in ensuring clinical trials are conducted safely, ethically and efficiently while building strong partnerships with investigators, study coordinators, pharmacists and sponsors.

The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor.

The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor.

As a CRA, you will play a critical role in ensuring clinical trials are conducted safely, ethically and efficiently while building strong partnerships with investigators, study coordinators, pharmacists and sponsors.

We're excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.

Responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

The Research Assistant – Clinical Neurosciences will contribute to clinical research activities through supporting the development, coordination and delivery of research projects. The role will support research protocols, clinical studies, data acquisition, data management, analysis and reporting activities while working collaboratively with researchers, clinical specialists and stakeholders.