Initiation Clinical Research Associate

Working from home with occasional days in our office location in Sao Paulo, as an Initiation Clinical Research Associate (ICRA) you will be the direct point of contact with assigned sites located throughout South America and accountable for quality and delivery during the start-up phase.  Duties will include Preparation, negotiation, and facilitation of Confidentiality Agreements (CDA), Informed Consent Forms (ICF) and EC submissions as well as maintaining appropriate Clinical Trial Management systems (CTMS) in a timely manner.

To be considered for this opportunity you must have clinical trials experience as study nurse or site coordinator ideally with a university degree in a health-related discipline.  Understanding of GCP and relevant regulations plus knowledge of submissions and ICF customizations is expected.  This is a virtual team environment, and your strong interpersonal and communication skills will help you to succeed.  Fluency in English is required.