Clinical Research Associate Jobs in Australia

Clinical Operations Team at Novotech drives innovative biotech clinical trials across early development and Phase I‑III studies. The Clinical Research Associate ensures trials are conducted safely, ethically and efficiently by independently managing site monitoring, building strong investigator relationships and driving patient recruitment.

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.

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.

PSI, a global clinical research organization, is seeking a Clinical Research Associate II to manage clinical aspects of global projects in Australia. The role involves conducting onsite monitoring, ensuring data compliance, and maintaining relationships with sites and investigators.

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.

Biopharma Site Management and Monitoring team at AstraZeneca builds and oversees high‑quality clinical trials. The Clinical Research Associate drives site activation, conducts risk‑based monitoring, and ensures data integrity and patient safety.

Precision Medicine Group is a CRO integrating clinical trial execution with advanced data sciences to accelerate oncology and rare disease therapies. The Senior/Clinical Research Associate oversees site management, conducts monitoring visits, ensures regulatory compliance, and supports data quality and patient safety across multiple studies.

Precision for Medicine is seeking a Senior/Clinical Research Associate to support study sites and clinical project teams in clinical research studies, with a strong focus on Oncology and Rare Disease. The CRA oversees site management, conducts on-site and remote monitoring visits, ensures data quality and regulatory compliance, and acts as the primary point of contact for investigators.

IQVIA seeks a Senior Clinical Research Associate to support the Clinical Research and Regulatory teams in North Sydney, NSW. The role involves maintaining Trial Master Files, managing clinical documentation, and assisting with site compliance tracking. This is a full-time position based on-site in 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 Research team at Covance conducts unblinded clinical studies. The Clinical Research Associate I monitors sites, ensures protocol compliance, manages data integrity and travel logistics.

Clinical Services – Clinical Study Delivery team ensures rigorous monitoring and site management for multinational clinical trials. The Sr. CRA leads monitoring services, mentors CRAs, oversees site recruitment, data integrity, and acts as primary liaison with sponsors and project 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.

Novotech is seeking a Clinical Research Associate (CRA II/III) for its Melbourne team to support Early Clinical Development and Phase I-III studies. 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.

Clinical Site Operations at Parexel ensures high‑quality clinical trial execution across Australia. The Clinical Research Associate II/Senior monitors investigator sites, manages study conduct from activation to database lock, and collaborates with study teams to resolve issues and ensure compliance.

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.

Novotech Clinical Research Team ensures trial participant safety and data integrity across diverse therapeutic areas. The Clinical Research Associate builds site relationships, monitors study compliance, drives participant recruitment, and supports regulatory submissions, working closely with investigators and internal CRO partners.

Global Clinical Operations at Allucent drives clinical trial execution for biopharma partners. As a Clinical Research Associate you will independently monitor investigational sites, ensure compliance with protocols, GCP and regulatory standards, and act as the primary liaison between sponsors and sites.

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.