A Clinical Research Associate (CRA) is a profession defined by Good clinical practice guidelines (ICH GCP). The main function of a clinical research associate is to monitor clinical trials. He or she may work directly with the sponsor company of a clinical trial, as an independent freelancer or for a Contract Research Organization (CRO). A Read more…
Auditor, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCPs), supporting a program of quality assurance (QA) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: Read more…
Requirements: CRA (Freelance) JOB SUMMARY Our client requires a CRA for a 12 month contract position. You will be working on ophthalmology study. This role is field (home based) and applicants will need to have extensive monitoring experience. Competitive rates. JOB TITLE CRA/Clinical Research Associate/Freelance/Contract LOCATION Field Based/Home Based BENEFITS Read more…