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 AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: 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/ _______________________ Contract research organisations (CROs) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech 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 Bachelor’s degree in a field directly related to the program responsibilities and one year of 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 company of a clinical trial, as an independent freelancer or for a Contract Research Organization (CRO). A Read more…
