1. 3 - 5 years of clinical research experience; 1 year specifically within oncology 2. Bachelor s degree required 3. Phase I clinical trial experience within a CRO environment. Note: The client has strong teams based in the TX, TN and GA areas. They have asked us to refer candidates from locations other than the TX, TN and GA areas.
Tell me about this job Perform routine site monitoring visits, participate in site selection, site initiation, and study closure activities to ensure that the clinical trial is being conducted according to the approved protocol, amendments and in compliance with Good Clinical Practice (GCP), corporate and/or Sponsor SOPs, and all applicable regulatory requirements. Apply Here: http: //relode. co/TO1B6GO or message us for additional details and personal attention.
