Sorumluluklar Bu dinamik Kanser Merkezi CTO ekibinin bir parçası olarak, Klinik AraÅŸtırma Koordinatörleri yönetecek & çeÅŸitli onkoloji klinik araÅŸtırmalarını denetlemek, çalışmanın baÅŸlangıcından bitiÅŸine kadar. Responsibilities for this position include but are not limited to: activation & maintenance of the oncology clinical trials protocols; acting as liaison between physicians, Devamı…
Phoenix Klinik AraÅŸtırma Berytech Teknolojisi & SaÄŸlık Åžam Yolu, Beyrut-Lübnan mobil : + 961 3 672 310 (Dr.. Georges Labaki) Ofis telefonu: + 961 1 429 566 info@phoenix-cr.com web sitesi – https://www.phoenix-cr.com/ _______________________ SözleÅŸmeli araÅŸtırma kuruluÅŸları (CRO'lar) Yazan: Peter Hogg ProKlinik YaÅŸam Bilimleri eczacılığın vazgeçilmezi haline geldi, biyoteknoloji, ve tıp teknolojisi Devamı…
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 Devamı…
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 Devamı…
Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH Ä°yi Klinik Uygulamaları: BirleÅŸtirilmiÅŸ Kılavuz,” (GCP'ler), Filigran tarafından yönetilen müşteri programlarının desteklenmesi, proje verilerinin ve özet beyanlarının bilinen ve belgelenen kalitede olmasını saÄŸlar. Requirements Will be expected to travel extensively to study Devamı…
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: BirleÅŸtirilmiÅŸ Kılavuz,” (GCP/GLP’s), bir kalite güvence programını desteklemek (KG) to ensure that Allergan project data and summary statements are of known and documented Devamı…
