CROPHA CAREERS

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. 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.

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, or be self-employed. Their work usually entails 50-70% travel and multiple investigational site visits.

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: