Regional CRA for immediate need. As key team members supporting new drug applications, the Regional CRA is accountable for on-site clinical monitoring activities from study start-up through close-out. As specified in the monitoring plans, the RCRA will perform source document verification review of Case Report Forms, oversee drug accountability, as well as manage investigational site to ensure compliance with FDA regulations, ICH/GCP guidelines, and company SOPs.
 

 
Requirements: Travel
 
These positions are home-based and require over 50% travel
 

 
Experience:
 
For you to be the successful candidate we are looking for in these roles you must have a proven track record of monitoring clinical trials in a variety of Therapeutic Areas through the CRO or Pharmaceutical industry
 

 
Education:
 
For consideration, you must hold a Bachelor’s degree, preferably in a scientific or nursing discipline Due to the precise requirements of these positions, we will only be contacting candidates that meet all of the listed criteria. If you are qualified and interested in the excellent career opportunities we have for you, please reply to this ad immediately with your CV and availability.