Clinical Research Associate Jobs in Australia

Clinical Research Associate 2 role at IQVIA involves monitoring clinical trial sites to ensure compliance with GCP and ICH guidelines. The associate conducts site visits, manages recruitment plans, administers protocol training, and maintains trial master files.

Clinical Research team at Bristol Myers Squibb ensures the integrity and compliance of clinical trial sites. The CRA conducts site qualification, monitoring, and close‑out visits, verifies data in electronic and paper records, and supports sites with training and risk mitigation.

Site Management and Monitoring teams across Oncology and Cell Therapy at AstraZeneca build and oversee high‑quality clinical trials. The Clinical Research Associate owns site activation and performance, conducts risk‑based monitoring, and ensures patient safety and data integrity through onsite and remote visits.

Site monitoring and management for clinical studies in Australia, ensuring compliance with SOPs, regulatory guidelines, and data integrity. Responsibilities include routine and closeout monitoring, CRF review, SAE reporting, travel management, and coordination with vendors and internal teams.

Clinical Research Associate 2 at IQVIA (formerly Quintiles IMS) is responsible for monitoring and site management across multiple protocols and therapeutic areas. The role includes performing site monitoring visits—selection, initiation, monitoring, and close‑out—ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

AstraZeneca is expanding its Biopharma and Oncology teams, hiring Clinical Research Associates to start in March/April 2026. The role focuses on site activation, risk‑based monitoring, and ensuring compliance with ICH‑GCP and local regulations.

Clinical Research Associate (CRAII-CRAIII) at Novotech ensures trial participant rights, data integrity, and GCP compliance. Acts as primary liaison between sites, Novotech, and sponsors, managing site relationships, recruitment, and monitoring across all trial phases.

Thermo Fisher Scientific’s Clinical Research Associate (Level I/II) team drives global clinical monitoring and site management for pharmaceutical and biotech trials. The role conducts risk‑based site monitoring, manages feasibility to close‑out activities, and ensures ICH‑GCP compliance across multiple sponsors.

Biopharma and Oncology teams at AstraZeneca are building high‑quality, patient‑centric clinical trials across therapeutic areas. As a Clinical Research Associate you will own site activation and performance, conduct risk‑based monitoring, ensure data integrity and patient safety, and partner with investigators to drive enrollment and inspection readiness.

Cell Therapy Site Management & Monitoring (SMM) at AstraZeneca partners with investigators to initiate, run and close advanced cell therapy studies, ensuring compliance and patient access. The CRA drives start‑up, monitoring visits, data verification and regulatory maintenance, collaborating with Local Study Managers and site staff.

Biopharma and Oncology teams at AstraZeneca design and deliver patient‑centric clinical trials across therapeutic areas. The Clinical Research Associate will own site activation and performance, conduct risk‑based monitoring, and ensure data integrity and patient safety through onsite and remote visits.

Cell Therapy Site Management & Monitoring (SMM) at AstraZeneca partners with investigators to initiate, run and close advanced cell therapy trials, ensuring compliance and rapid patient access. As a Clinical Research Associate you’ll manage start‑up, monitoring visits, data verification and regulatory documentation for Australian sites, collaborating with Local Study Managers and using Veeva Clinical Vault.

Site Management and Monitoring team at AstraZeneca builds and oversees oncology and cell therapy clinical trials. The Clinical Research Associate activates sites, conducts risk‑based monitoring, ensures data integrity and patient safety, and prepares sites for inspections.

Clinical Research Associate 2 role focused on site visits, recruitment strategies, and study progress monitoring. Requires a life sciences degree, 18 months of monitoring experience, and knowledge of GCP and ICH guidelines.

Clinical Research Associate 2 role focused on site visits, recruitment, training, and study monitoring. Requires life sciences degree, 18+ months of monitoring experience, and GCP knowledge.

We are seeking a Clinical Research Associate II to manage and monitor clinical trials across Melbourne, Adelaide, and Perth. The role involves site management per SOPs and ICH GCP, conducting initiation, monitoring, and close‑out visits, and preparing monitoring plans.

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.

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.

Join the Australasian Kidney Trials Network as a Clinical Research Associate to coordinate multi‑centre trials, support protocol development, monitor site performance, ensure GCP compliance, and drive high‑quality research across Australia, New Zealand and beyond.

Fortrea, a leading global contract research organization, seeks a Clinical Research Associate II to support clinical trials across diverse therapeutic areas. The role involves monitoring study sites, ensuring protocol compliance, managing data integrity, and coordinating travel and expenses.