WHAT IS A CRA?

A Clinical Research Associate (CRA), sometimes referred to as a Monitor, is someone who oversees the progress and conduct of a clinical trial/investigation. The CRA is responsible for assuring:

  • the protection of rights, safety and well being of human study subjects;
  • that regulations are met;
  • the protocol is followed and data is reported accurately;
  • that ethical practices are employed at all investigational sites participating in a clinical study and that the scientific integrity of the data is upheld.

Activities are conducted off-site (remote), on-site (investigational site) or both.

WHO CAN BECOME A CRA?
A CRA usually has a health care or science background (e.g. nurse, Bachelor’s, Masters or Ph.D. in a science). They may be employed by a Pharmaceutical Company, a CRO, a staffing company or be self-employed.

LET CROPHA ADD VALUE TO YOUR CAREER

Join us and make a difference as a CRA. CROPHA is always looking for experienced and reliable Clinical Research Associates as well as junior CRAs and motivated people looking to get started as a CRA. If you are fluent in English, French and/or Dutch, and would like to join a growing and dynamic CRO, please fill in our online application form or send your CV to: info@cropha.com

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