clinical research associate
عنوان: Pubic Health – 2024 AGENDA Beginning of the registration — 09:30 a.m. Opening of the conference — 10:00 a.m. Plenary meeting 10:00-12:30 Opening part • The role of radiological research in providing quality medical services to people • Rational approach to equipping medical institutions with radiology equipment اقرأ المزيد
Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (دكتور. 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 اقرأ المزيد
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, ادارة الاغذية والعقاقير, إما )Модуль 2. Этические аспекты КИ Принципы биоэтики и этические комитетыДекларация ХельсинкиПроцедура получения информированного согласия اقرأ المزيد
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 (كرو). أ اقرأ المزيد
مدقق حسابات, 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: اقرأ المزيد
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 اقرأ المزيد
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 اقرأ المزيد
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 اقرأ المزيد
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, اقرأ المزيد