clinical trials
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 Read more…
Contract research organisations (CROs) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech industries by supporting clients’ efforts to test, refine, and market the latest pharmaceuticals and medical Read more…
Responsibilities Duties: The Clinical Research Administrator reviews applications for research projects to ensure that protocols meet regulatory and ethical standards for the protection of human or animal subjects. Requirements Minimum Requirements: This position requires a Read more…
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 Read more…
