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How to Become a Clinical Research Associate

Introduction

Clinical research associates (CRA) do not have very difficult jobs. Many CRAs were originally clinical research coordinators that are now seeking a career change. CRAs are responsible for verifying that data that was inserted by an investigator’s site staff is correct. CRAs must also make sure that the data adheres to protocol. They need to be well versed in the laws and regulations that govern clinical trials. CRAs must receive certification from an accredited source in order to find employment.

Difficulty: Easy

Things You'll Need:

- Resume

- Internet access

Instructions

Step 1

Shadow a current clinical research associate. This will help you decide if this career is right for you. You can also take a class that will provide you with on-the-job training to help you make your decision.

Step 2

Revise your resume to highlight skills that will land you a job as a clinical research associate. Emphasize any experience that you have in entering and verifying data. Read CRA job descriptions and cater your resume towards highlighting the proficiencies that you have that are required of CRAs.

Step 3

Understand your job. CRAs are responsible for enforcing the sponsor’s procedure. CRAs must also ensure that federal rules and international regulations are followed.

Step 4

Familiarize yourself with the terms and processes of the pharmaceutical industry. The internet is a good resource for finding this kind of information. You can enroll in courses or sign up for forums that are connected to Good Clinical Practices (GCP).

Step 5

Apply for certification. Try to obtain certification from the ACRP or the SOCRA. You can find information about these organizations and their certification procedures on their websites.

Tip

Network with current CRAs because in this field you can find jobs easily through connections.

Warning

Remember that even licensed medical professionals need GCP certification to be CRAs.