clinical research associate | Terapia cu celule stem & Medicina Regenerativa

ТРЕНИНГ: Организация клинических исследований и сертификация специалиста по проведению КИ

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 (ICH-GCP, FDA, EMA )Модуль 2. Этические аспекты КИ Принципы биоэтики и этические комитетыДекларация ХельсинкиПроцедура получения информированного согласия Citeşte mai mult

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cercetare clinică

Coordonator de cercetare clinică în vizită

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, Citeşte mai mult

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Auditor GCP

Senior Clinical Research Associate

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 Citeşte mai mult

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Auditor GCP

Director, GCP

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 Citeşte mai mult

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cercetare clinică

Clinical Research Administrator

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 Citeşte mai mult

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Auditor GCP

Auditor, GCP

Auditor, 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: Citeşte mai mult

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cercetare clinică

CRA certification

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). O Citeşte mai mult

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2018 Conferințe de anestezie

Public Health -2024, medical congress

Titlu: 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 Citeşte mai mult

De NBScience, 2 săptămâniaugust 17, 2026 în urmă

practica clinica

Top Contract research organisations (CROs) . Listing

Top Contract Research Organizations (CROs) in Europe: Clinical Research and the Rise of Regenerative Medicine (2026 Guide) Meta Description:Explore top CROs in Europe and discover how clinical research is evolving toward regenerative medicine, including autologous mesenchymal stem cells in Barcelona, Spania. The Role of CROs in Modern Medicine Contract Research Citeşte mai mult

De NBScience, 2 săptămâniaugust 17, 2026 în urmă