associé de recherche clinique
A Clinical Research Associate (ARC) is a profession defined by Good clinical practice guidelines (Je 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). UN Lire la suite
Auditeur, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, « ICH Good Clinical Practice: Ligne directrice consolidée, » (GCP), soutenir un programme d’assurance qualité (Assurance qualité) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: Lire la suite
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 Lire la suite
Responsibilities The Director, GCP sera tenu de tout superviser et de participer à, audit d’assurance qualité de toutes les activités soumises à la, « ICH Bonnes pratiques cliniques/de laboratoire: Ligne directrice consolidée, » (BPC/BPL’s), soutenir un programme d’assurance qualité (Assurance qualité) to ensure that Allergan project data and summary statements are of known and documented Lire la suite
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 Lire la suite
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, Lire la suite
Titre: Santé publique – 2024 ORDRE DU JOUR Début des inscriptions — 09:30 suis. Ouverture de la conférence — 10:00 suis. Réunion plénière 10:00-12:30 Partie d'ouverture • Le rôle de la recherche radiologique dans la fourniture de services médicaux de qualité aux personnes • Approche rationnelle pour équiper les établissements médicaux en équipements de radiologie Lire la suite
Technologie Berytech de recherche clinique Phoenix & Santé Route de Damas, Beyrouth-Liban mobile : + 961 3 672 310 (Docteur. Georges Labaki) numéro de bureau: + 961 1 429 566 Site [email protected] – https://www.phoenix-cr.com/ _______________________ Organismes de recherche sous contrat (CRO) par Peter Hogg Les sciences de la vie ProClinical sont devenues essentielles à l'industrie pharmaceutique, biotechnologie, et technologie médicale Lire la suite
Организация клинических исследований и сертификация специалиста по проведению КИМодуль 1. Введение в клинические исследования (КИ) История и развитие клинических исследованийОсновные понятия и терминологияТипы и фазы клинических исследований (Phase I-IV)Международные и локальные регуляторные требования (I-GCP, FDA, EMA )Модуль 2. Этические аспекты КИ Принципы биоэтики и этические комитетыДекларация ХельсинкиПроцедура получения информированного согласия Lire la suite