Clinical Research Associate

A Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory standards and protocols. This role involves working closely with clinical sites, coordinating with investigators, and ensuring that data is collected accurately and ethically.

CRAs conduct regular site visits, review trial documentation, and provide training to site staff on study protocols. Additionally, they play a key role in reporting trial progress and addressing any issues that arise during the research process.

Future demand High
Average yearly income $95,992
Skill level Unknown

How do I become a clinical research associate?

All skill levels Beginner Experienced

Bachelor of Science (Pharmacology)

Blended, On Campus
3 years
$0 - $123,300
  • There are no mandated entry requirements.
Additional requirements may apply.
  • There are no mandated entry requirements.
Additional requirements may apply.

Bachelor of Biomedical Science (Pharmacology)

On Campus
3 years
$0 - $27,401
  • There are no mandated entry requirements.
Additional requirements may apply.
  • There are no mandated entry requirements.
Additional requirements may apply.
*Showing course fees for all providers. Some providers may not be available in your area.

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Further reading

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What can you do with a Diploma of Clinical Coding?

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