klinischer Forschungsmitarbeiter
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 (CRO). A Weiterlesen
Wirtschaftsprüfer, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, „ICH Good Clinical Practice: Konsolidierte Richtlinie,“ (GCPs), Unterstützung eines Programms zur Qualitätssicherung (Qualitätssicherung) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: Weiterlesen
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 Weiterlesen
Responsibilities The Director, GCP wird verpflichtet sein, alles zu überwachen und sich daran zu beteiligen, Qualitätssicherungsprüfung aller Tätigkeiten, die dem unterliegen, „ICH Gute klinische/Laborpraxis: Konsolidierte Richtlinie,“ (GCP/GLPs), Unterstützung eines Programms zur Qualitätssicherung (Qualitätssicherung) to ensure that Allergan project data and summary statements are of known and documented Weiterlesen
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 Weiterlesen
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, Weiterlesen
Titel: 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 Weiterlesen
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 Weiterlesen
Организация клинических исследований и сертификация специалиста по проведению КИМодуль 1. Einführung in die klinische Forschung (WER) История и развитие клинических исследованийОсновные понятия и терминологияТипы и фазы клинических исследований (Phase I-IV)Internationale und lokale regulatorische Anforderungen (ICH-GCP, FDA, EMA )Modul 2. Этические аспекты КИ Принципы биоэтики и этические комитетыДекларация ХельсинкиПроцедура получения информированного согласия Weiterlesen