Clinical Research Associate Jobs in Victoria, Australia

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.

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.

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.

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

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.

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.

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.

The role: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Are you a Clinical Research Associate looking for your next big adventure? Look no further than IQVIA, a global CRO with outstanding reputation.

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.

The UAB Huntsville Medical Campus-Research is seeking a Clinical Research Coordinator I to support a mental health clinical trials clinic. The role involves organizing patient enrollment planning, compiling and analyzing data, maintaining records, tracking progress, and conducting quality assurance on data collected for studies involving patients with serious mental health disorders.

As the Clinical Research Fellow within the Oncology Department at St Vincent’s Hospital, Melbourne, you will provide direct medical care to assigned clinical trial patients under the supervision and guidance of a Senior Staff Specialist. You will assist in identifying patients potentially eligible for clinical trials, assist in consenting and coordination of tissue for studies involving molecular screening, and undertake clinical trial procedural work including oversight of ethics submissions, t

The National Centre for Infections in Cancer (NCIC) at the Peter MacCallum Cancer Centre is seeking an Infectious Diseases - Clinical Research Fellow to provide clinical oversight for patients in infection-related trials while advancing research, education, and service development. Day-to-day work includes coordinating clinical trial activities, supporting protocol development, ethics and governance submissions, managing research data, screening and consenting patients, capturing adverse events,

Join our team as a Clinical Research Coordinator on a 0.6FTE, fixed term (ending Dec 2028) to work at MCHRI based at Clayton.The Clinical Research Coordinator will provide research and administrative support to the iIMPROVE group at Monash Emergency Research Collaborative (MERC), working closely with senior research staff to support the delivery of clinical research projects within the implementation science framework. The role will contribute to study coordination, data management, ethics and g

The Parkville Cancer Clinical Trials Unit (PCCTU) co-ordinates clinical trials across the 3 institutions of the Parkville Medical precinct: The Peter MacCallum Cancer Centre, the Royal Melbourne Hospital and the Royal Women’s Hospital. We are the largest oncology trials unit in Australia with an exciting and expanding trials portfolio.

Are you an experienced Clinical Research Trial Coordinator looking to make a meaningful difference in cancer research? An exciting opportunity is available to join the Jreissati Pancreatic Centre at Epworth , supporting a growing portfolio of pancreatic cancer clinical trials.

In Vivo Pharmacology team at Moderna develops autoimmune and inflammatory disease models to advance mRNA therapeutics. The Senior Research Associate executes in‑vivo studies, performs dosing, sample collection, and data analysis, while collaborating on study design and troubleshooting.

Moderna’s Infectious Disease Research Immunology team seeks a Sr. Research Associate to advance vaccine and therapeutic candidates from preclinical through IND-enabling studies. The role focuses on designing, executing, and optimizing antibody binding and functional serological assays to characterize humoral immune responses.

Moderna is seeking a Manufacturing Associate II to join Research Analytics – High Throughput Operations in Cambridge, MA. This hands-on, on-site role supports the reliable, reproducible, and timely production of DNA, mRNA, and Lipid Nanoparticle (LNP) materials used across Moderna’s research portfolio. The Manufacturing Associate II independently executes established high-throughput workflows, operates manual and automated laboratory systems, documents work accurately, and applies process knowle

Moderna is seeking a Senior Research Associate to join the Protein Design team at its Cambridge, MA site. This role will support protein expression, purification, and biophysical characterization efforts for Infectious Disease Research vaccine and therapeutic programs.