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…
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…
Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (Dr. Georges Labaki) office number: + 961 1 429 566 info@phoenix-cr.com website – https://www.phoenix-cr.com/ Read more…
