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 projected growth of the Clinical Research Associate (CRA) position in Canada shows promising trends in the job market. Over the past 10 years, there has been a steady increase in employment opportunities for CRAs. According to recent data points from Google, the demand for CRAs is expected to grow significantly in the coming years. With an increasing focus on healthcare advancements and medical research, the demand for skilled CRAs is predicted to rise. This growth is anticipated to create a substantial number of employment opportunities for individuals in the field, ensuring a promising career outlook for aspiring CRAs in the Canadian market.

How to Learn

As a Clinical Research Associate CRA with 0-3 years of experience in Canada, your main responsibilities include:<ul><li> Conducting site initiation visits, ensuring compliance with study protocols, and training site staff on study procedures.</li><li> Monitoring data collection, ensuring accurate and timely entry of study data, and resolving data discrepancies.</li><li> Assisting in the preparation and review of study documents, including informed consent forms and study protocols.</li><li> Collaborating with study coordinators, investigators, and sponsors to ensure the smooth execution of clinical trials and adherence to regulations and guidelines.</li></ul>

Roles & Responsibilities

Average take home Salary for a Clinical Research Associate (CRA) in Canada is around C$68688 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

Skills That Affect Clinical Research Associate (CRA) Salaries

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