Clinical Research Associate Jobs in Victoria, Australia

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.

IQVIA’s Clinical Research Associate Trainee Program in Melbourne trains new talent in clinical trial monitoring, covering site selection, initiation, monitoring, and close‑out. Trainees learn ICH‑GCP and Australian regulations, conduct supervised site visits, manage study progress, and maintain Trial Master Files.

Novotech’s Clinical Research Associate (CRA II/III) team in Melbourne drives the execution of clinical trials, ensuring participant safety and data integrity. The role manages site relationships, conducts monitoring visits, and supports regulatory submissions, all while maintaining GCP compliance.

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.

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.

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.

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.

Clinical Research Associate II role at Covance (Fortrea) in Melbourne involves overseeing all aspects of site monitoring for global clinical trials, from pre-study visits to close-out. Responsibilities include maintaining study files, ensuring protocol compliance, reviewing CRFs, managing audit readiness, and handling travel logistics per Fortrea policy.

Fortrea, a leading global contract research organization, seeks a Clinical Research Associate II based in Melbourne to oversee site monitoring, data integrity, and regulatory compliance across clinical trials. The role involves routine and close‑out monitoring, protocol training, CRF review, audit readiness, and travel management.

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.

ProPharma Group seeks a Senior Clinical Research Associate to join our team on a 0.2 FTE basis, contributing to high-quality clinical research projects. The role involves conducting site monitoring visits, ensuring data integrity, and maintaining strong relationships with investigational sites.

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

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.

Senior Clinical Research Associate I is responsible for monitoring and managing clinical study sites, ensuring compliance with SOPs and regulatory guidelines. The role includes routine site visits, closeout, file maintenance, and vendor liaison.

Lead CRAs will be assigned to different studies conducted in one or more countries to deliver and progress the assigned studies. The Lead CRAs will also be assigned as CRA to one study site as a minimum to verify an adequate understanding of sponsor requirements, procedures, and systems.

Senior Clinical Research Associate I (SCRA1) at Covance (Fortrea) oversees site monitoring and management for clinical studies. Responsibilities include routine monitoring, closeout, file maintenance, pre‑study and initiation visits, vendor liaison, and other duties.

Senior Clinical Research Associate at IQVIA (formerly Quintiles IMS) drives innovation and excellence in clinical research. The role focuses on site visits, recruitment, training, quality assurance, study monitoring, documentation, financial oversight, and team collaboration across multiple Australian locations.

Senior Clinical Research Associate I responsible for site monitoring and management across clinical studies, ensuring compliance with SOPs and regulatory guidelines. Leads limited-scope projects, performs routine monitoring, closeout, and site management tasks, liaises with vendors, and supports study operations.

Medtronic invites recent graduates with a Bachelor’s Degree in Nursing, Biomedical or Health Sciences to join the Clinical Research Team in Richmond, Victoria. The Graduate Clinical Research Associate role offers a dynamic, year‑long program where you’ll support the execution of Medtronic clinical trials, assist with research, and coordinate non‑technical projects.