Terapia com células -tronco na Ucrânia

Clinical Research Associate/Clinical Research Coordinator

Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCPs), supporting client programs administrated by Watermark ensure project data and summary statements are of known and documented quality. Requirements Will be expected to travel extensively to study Ler mais…

Terapia com células -tronco na Ucrânia

Director, GCP

Responsibilities The Director, GCP will be required to oversee all and participate in, quality assurance auditing of all activities subject to the, “ICH Good Clinical/Laboratory Practice: Consolidated Guideline,” (GCP/GLP’s), supporting a program of quality assurance (QA) to ensure that Allergan project data and summary statements are of known and documented Ler mais…

Terapia com células -tronco na Ucrânia

Senior Clinical Research Associate

Responsibilities Assisting in the design and execution of high quality clinical studies in compliance with FDA and ICH requirements. Function as a primary liaison to clinical investigators/site staff. Identify, qualify, initiate, monitor and close out clinical sites. Co-monitor with CRO when issues arise with the site. Assist in the selection Ler mais…

Terapia com células -tronco na Ucrânia

Top Contract research organisations (Cros) . Listing

Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (Dr. Georges Labaki) office number: + 961 1 429 566 [email protected] 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 Ler mais…