A Clinical Research Associate (CRA) is a highly skilled and trained professional who plays a crucial role in the development and execution of clinical trials. As a CRA, their primary responsibility is to ensure that studies conducted on human subjects adhere to all applicable regulations, guidelines, and protocols. They work closely with the study sponsor and investigators to monitor the progress of clinical trials and collect data in an organized and valid manner. CRAs are responsible for conducting site initiation, monitoring visits, and closeout visits at various study sites, ensuring that all necessary documentation and records are accurate and complete. They assure data integrity, patient safety, and well-being by performing site qualification, initiation, routine monitoring, and closeout visits, ensuring that the clinical trial is conducted in accordance with the approved protocol and regulatory requirements. Additionally, they review and verify the data collected, prepare monitoring reports, and communicate with the study team and investigators regarding any issues or concerns. CRAs are also responsible for maintaining study files and ensuring the timely and accurate completion of all study-related documents. In summary, a Clinical Research Associate plays a critical role in the successful planning, execution, and completion of clinical research trials, with a high level of attention to detail and adherence to regulatory and ethical standards.

The job role of a Clinical Research Associate (CRA) in Australia is projected to experience significant growth in the market. According to a 10-year analysis, there is an increasing demand for CRAs due to the expansion of clinical research activities in various sectors such as pharmaceuticals, biotechnology, and medical devices. With advancements in healthcare and the need for drug development, the employment opportunities for CRAs are expected to rise in the coming years.

How to Learn

As a Clinical Research Associate CRA with 0-3 years of experience in Australia, your main responsibilities include:<ul><li> Conducting site initiation visits, ensuring compliance with protocols, and providing training to site staff. You will visit research sites, ensure they meet the study requirements, train the staff, and ensure protocol compliance.</li><li> Monitoring clinical trials, reviewing study data, and resolving data discrepancies. You will monitor ongoing trials, review data collected, and resolve any inconsistencies or discrepancies.</li><li> Assisting in the preparation and submission of regulatory documents and ethics committee approvals. You will help in preparing and submitting necessary documents and obtaining approvals from regulatory bodies and ethics committees.</li><li> Maintaining study files, tracking study supplies, and ensuring adherence to good clinical practice GCP guidelines.</li></ul>

Roles & Responsibilities

Average take home Salary for a Clinical Research Associate (CRA) in Australia is around $49591 per year

Salary Breakup

Clinical research associates (CRA) are accountable to assist in the process of conducting clinical research, offering advanced technical assistance in areas such as handling equipment, ordering tests, and presenting results, specific research data to the general public, and various administrative tasks. CRAs must adhere to strict safety and privacy regulations to avoid problems with their subjects and ethical concerns They must also organize themselves and give careful attention to the finer points when conducting research using investigative techniques in healthcare or clinical settings.

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Clinical Research Associate (CRA)

Salary Breakup

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