MackShah02

· 21 Mar 2024

Follow Following

Job Role and Responsibilities of Clinical Research Associate

The world is developing around and Biotechnology touches every aspect of our daily life chores directly or indirectly. With time, the demand for innovative technologies is increasing, leading to a vast number of jobs in Biotechnology. In this article, we will talk about the roles and responsibilities of a Clinical Research Associate. A Clinical Research Associate or CRA in clinical operations is accountable for setting up, coordinating and supervising clinical studies.  

One has to plan, prepare and help in the execution of the clinical trials to test new or existing investigational products. This evaluates their safety and the advantages of use. The work is usually done within pharmaceutical companies or CROs who manage clinical research on behalf of pharmaceutical companies. Studies are also needed within hospital departments that collect information about investigational products.

You are the initial contact for several parties, including doctors, researchers, laboratories, pharmacists, ethics committees and others such as the sponsor or client. In short, as a Clinical Research Associate, you are accountable for ensuring that all the risks and effects of investigational products have been fully evaluated and approved before their release in the market.

Curious about other clinical jobs or looking for a starter's job? Take a look at www.biostaffic.com! 

The CRA position is vast and dynamic. Particular duties can differ depending on the company, and you may work on multiple projects. A CRA will commonly be required to:

• Execute selection, initiation, monitoring and close-out visits at the participating clinical trial sites, also for logistics and coordination of the study;

• Monitor the study to check whether it has been carried out according to the applicable laws and regulations;

• Develop study procedures, methodology and instructions for clinical trials staff and for design data collection tools;

• Handle study supplies, medication supplies and medication accountability;

• Collect, verify and finalize collected data to make reports and present results of findings to other medical staff;

• Ensure the safety and well-being of test subjects by working with ethics committees;

• Clinical trial documents are submitted for review and approval by those ethics committees.