Responsibilities As part of this dynamic Cancer Center CTO team, Clinical Research Coordinators will manage & oversee several oncology clinical trials, from study inception to termination. Responsibilities for this position include but are not limited to: activation & maintenance of the oncology clinical trials protocols; acting as liaison between physicians, Per saperne di più…
Tecnologia Berytech per la ricerca clinica di Phoenix & Salute Damasco Road, Cellulare Beirut-Libano : + 961 3 672 310 (Dott. Georges Labaki) numero dell'ufficio: + 961 1 429 566 sito web info@phoenix-cr.com – https://www.phoenix-cr.com/ _______________________ Organizzazioni di ricerca a contratto (CRO) di Peter Hogg Le scienze della vita procliniche sono diventate essenziali per l'industria farmaceutica, biotecnologia, e tecnologia medica Per saperne di più…
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 Per saperne di più…
NBScience _____________________________ fornisce soluzioni intelligenti per le industrie della ricerca clinica NBScience offre ai clienti un'ampia gamma di servizi nel settore della ricerca clinica. Offriamo per i nostri Clienti soluzioni di servizio completo relative alla parte clinica dello studio. Possiamo anche occuparci di IMP e altro Per saperne di più…
Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCP), 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 Per saperne di più…
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 Per saperne di più…
