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
NBScience ___________________________ providing smart solutions for clinical research industries NBScience offering to Clients wide range of services in the area of clinical research industry. We offer for our Clients full service solutions related to the clinical part of the study. We can also take care about IMP and other 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
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: Guía consolidada,» (GCP/GLP’s), apoyar un programa de garantía de calidad (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