Accelsiors is looking to hire a full time Clinical Research Associate (CRA).
The CRA acts as primary individual responsible for monitoring activities with investigational sites, from site identification and selection, through site activation, subject enrolment and study conduct until close out, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and any applicable regulations and SOPs.
By sending you CV, you consent to the processing of your personal data.
Your CV will be included in Accelsiors’ database to be considered for future roles.
If you are interested in the position and you agree with the above, please send us your CV in English to m.blanco@accelsiors.com
Further details in the attached file.