clinical research associate
Un asociado de investigación clínica (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 Leer más
Auditor, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, «ICH Good Clinical Practice: Consolidated Guideline,» (GCP), supporting a program of quality assurance (control de calidad) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: Leer más
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 Leer más
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 (control de calidad) to ensure that Allergan project data and summary statements are of known and documented Leer más
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 Leer más
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, Leer más
Título: Salud púbica – 2024 ORDEN DEL DÍA Inicio de la inscripción — 09:30 soy. Apertura de la conferencia — 10:00 soy. Sesión plenaria 10:00-12:30 Parte inicial • El papel de la investigación radiológica en la prestación de servicios médicos de calidad a las personas • Enfoque racional para equipar las instituciones médicas con equipos de radiología Leer más
Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (Dr. Georges Labaki) numero de oficina: + 961 1 429 566 [email protected] website – https://www.phoenix-cr.com/ _______________________ Contract research organisations (CRO) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech Leer más
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 Leer más