Clinical Research Associate 
– USA West Coast
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!
TRIO is seeking CRA positions on the west coast USA.
TRIO (Translational Research in Oncology) is an academic clinical research organization that is dedicated to advancing translational cancer research by pursuing forward innovative and targeted therapeutic concepts in the clinical trial setting.
We are committed to providing treatments of the future to the world of today.
We are looking for a Clinical Research Associates to join our international team, home-based in the USA.
Our CRAs play a pivotal role in moving our important research forward and helping to save cancer patients’ lives all over the world.
TRIO’s head office is in Edmonton, Alberta with operations throughout Canada, the USA, France and Uruguay.
The main objective of the Monitoring Resources team is to effectively monitor TRIO’s clinical trials according to contractual obligations and project deadlines according to the sponsor protocol and in compliance with the appropriate SOPs.
 Reporting to a Monitoring Resources Coordinator, a CRA is responsible for the following:  
    Conducting site visits, including pre-study, initiation, monitoring and termination;       Confirming adherence to all FDA, ICH-GCP and local regulations;       Ensuring the completion and collection of regulatory documents;       Performing data verification of source documents;       Ensuring implementation and compliance with FDA, ICH-GCP guidelines;       Participating in budget negotiation and follow-up where applicable;       Assisting with data validation and query resolution;       Mentoring junior team members as required.
  Qualifications:   
     A  minimum   of  2  years   of monitoring   experience in oncology trials           An advanced level of oncology knowledge           Completion of a science-related Bachelor’s degree           Excellent     knowledge     of     medical     terminology     and     clinical     monitoring     process           Strong   ICH-GCPs   knowledge            Experience   with clinical trial information systems          Ability to travel up to 60% on average     
  What we can offer you:   
     3 weeks of vacation          10 personal days         TRIO contributes 5% of your salary to 401(K)          Extended Health, Vision, Dental, Life and Disability Coverage for you and your family paid 100% by TRIO       How many years of monitoring experience do you have?* 
 How would you rate your oncology knowledge*