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How to become Clinical Research Associates (CRA) in Canada

Clinical Research Associate (CRA) plays a significant role in managing the process and organizing the information on clinical projects. Yet, it is difficult to become a Clinical Research Associates straight away, but, are you keen on a career that allows you to grow your skills and knowledge? Are you interested in starting a career in the clinical research industry? Are you keen on a career that requires you to take more responsibilities to ensure clinical trials are conducted ethically? If you answer yes to these questions without doubt, then working as a Applied Clinical Research Associate (CRA) may be the right choice for you!

What is the Career Outlook for Clinical Research Associates (CRA)?

As the healthcare industry is growing rapidly and prosperously, there are increasing career opportunities provided to people. According to research, particularly for clinical research associates, employment is expected to grow 7% between 2019 and 2029, and the median salary in 2019 was $61,269. The salary ranges of this profession are varied based upon the level of education, years of experience, and most importantly, whether you have done any clinical research training, or post-graduation diploma, or other certifications. That said, if you do not have a relevant educational background, and; want to get an entry-level career in clinical research, it is suggested to have a post-graduate diploma as it can guide and train you with the skills and experience needed in the field.

What are the Responsibilities for Applied Clinical Research Associates (CRA)?

Clinical Research Associates have key responsibilities to monitor and oversee clinical trial activities on a daily basis setting and providing a vital role throughout the study. In addition to running clinical trials, they need to coordinate to collect, distribute and analyze the data obtained during the trial process. However, there are many more responsibilities involves in a Clinical Research Associates role. Let’s take a look at a few key responsibilities:

  1. To make sure the conduct of the trial complies with the most recent approved protocol, with applicable regulatory authority requirements.
  2. To maintain a current understanding of the organization’s standard operating procedures.
  3. To prepare an Ethical Committee document for submission before clinical site initiation.
  4. To plan and conduct pre-study site evaluation visit with senior Clinical Trial Monitor.
  5. To provide clinical study progress reports to the Clinical Trial Manager regularly.
  6. To attend and assist with Investigator Meeting for training materials, logistic preparation, and coordination.
  7.  To keep track of patient recruitment procedures and monitor patient informed Consent progression for a clinical study.
  8. To follow up with the clinical site for the resolution of DCFs or any queries periodically.

How to Start your Career as Clinical Research Associate (CRA)?

By providing exceptional theoretical, technical, and hands-on experience with industry professionals, Bay River College’s Applied Clinical Research Post Graduate Program prepares students to contribute to and succeed in the field of clinical research. Through this 40 weeks program, students will learn diverse theories and models, in-depth analysis, and quality reassurance required for clinical research operations. As well, students will have the opportunity to work alongside industry professionals to leverage their expertise. Upon graduation, students will equip to make the transition from college to work and to achieve their ambitions effectively.

Apply Now in Our Applied Clinical Research Post-Graduate Diploma

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