Clinical Research Associate Jobs

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A clinical research associate or CRA is the person who is responsible for various types of jobs such as setting up, monitoring, and completing clinical trials. This is a desired job profile by the people who are experts in clinical research coordination. If you are keen on switching careers, it will help if you are familiar with the rules and regulations as well as the protocol requirements that govern the clinical trials. You can start with preparing a good resume with the basic understanding to know all about performing the tasks that are generally related to clinical research coordination.

The job profile and responsibilities of the clinical research associate includes delegating tasks that concern the maintenance and upkeep of the databases. The clinical research associate jobs require that the data that you are entering is accurate and precise. You are also required to verify that the data that is entered by the site staff of the investigator is precise and complies with the protocol. The clinical research associate jobs also need the person to be focused on the terminology of the common acronyms of the industry. Make sure you have all the required skills for the CRA jobs.

The academic qualifications for the CRA jobs are an academic or for that matter a bachelor's degree in Life Sciences along with a good understanding of the local regulations and good clinical practices. You can also go for clinical research associate degrees with the following subjects as well:


  • Biochemistry
  • Anatomy
  • Dentistry
  • Micro biology
  • Medicine
  • Biology
  • Biomedical science
  • Toxicology
  • Physiology
  • Immunology
  • Molecular biology
  • Pharmacology
  • Pharmacy
The clinical research associate monitors clinical trials by working as well as corresponding directly with the clinical trial sponsor company as a freelancer or for a contact research organization or CRO. The skills of a clinical research associate are to ensure that the facts are compliant with the following:
  • Clinical trial protocol
  • Checking of the activities of the clinical site
  • Making on site visits
  • Reviewing case report forms or CRF
  • Communicating with the clinical research investigators
You can sign up for the classes that are concerned with forums that are related to Good Clinical Practices or GCP. This will help you gain familiarity with the common terms that are used in the industry as well as the procedures of the pharmaceutical industry. You must also become a pro at the concerns of the clinical research associate industry and the ongoing trends and practices of the clinical research associates job.

Prior experience is important in CRA jobs as it helps you determine whether you are comfortable with the monitoring processes. This is in contrast to the functions of the clinical research coordinator as you are required to take classes that are hands on for providing CRA work that exposes you to the monitoring experience. The clinical research associate requires having an experience in networking as it helps them gain contacts and valuable recommendations.

The global career prospects of the clinical research associate or CRA jobs are good and they even vary between the companies, although a few companies also have motivational requirements available to the applicants and candidates. There are 3 levels of the CRA jobs and these include the following:
  • Visiting the investigative centers
  • More involvement in activities like protocol development and various kinds of coordination
  • Management of projects
You can get better jobs with experience and knowledge and thus your salaries can be significantly increased.

The median CRA salary for the clinical research associate per year is from $50,000 to $62,000, although this is something that depends on the organization, company, and experience of the candidate. The United States Bureau of Labor Statistics has affixed that the prospects are likely to be better until the year 2014.

The role of the clinical research associate involves stepping outside the box and adjusting your thought processes. In fact, with the growth and scope of your job, the priorities will also change and your job will be to focus on the protocol of the sponsor. As a clinical research professional, you will also need to adhere to the international guidelines as well as federal protocols. The CRA salary is also agreeable if you have the right educational qualifications and experiences that are required for the job.
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