Sorumluluklar Direktör, GCP'nin herkesi denetlemesi ve katılması gerekecek, tabi olan tüm faaliyetlerin kalite güvence denetimi, “ICH İyi Klinik/Laboratuvar Uygulamaları: Birleştirilmiş Kılavuz,” (GCP/GLP'ler), bir kalite güvence programını desteklemek (KG) Allergan proje verilerinin ve özet beyanlarının bilinmesini ve belgelenmesini sağlamak Devamı
Sorumluluklar Yüksek kaliteli klinik çalışmaların FDA ve ICH gerekliliklerine uygun olarak tasarlanması ve yürütülmesine yardımcı olmak. Klinik araştırmacılar/tesis personeli için birincil irtibat noktası olarak işlev görme. Tanımlamak, hak kazanmak, başlatmak, Klinik sahalarını izleyin ve kapatın. Siteyle ilgili sorunlar ortaya çıktığında CRO ile birlikte izleme. Seçimde yardımcı olun Devamı
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, 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
Başlık: 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 Devamı
Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (Dr.. Georges Labaki) ofis numarası: + 961 1 429 566 [email protected] website – https://www.phoenix-cr.com/ _______________________ Contract research organisations (CRO'lar) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech Devamı
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 Devamı