und kontinuierlichen Verbesserung der globalen Clinical Trial Supply Prozesse und Lieferketten Vertretung des Bereichs Clinical Trial Supply (CTS) gegenüber relevanten internen und extern Stakeholder und Unterstützung der Abteilungsleitung

und kontinuierlichen Verbesserung der globalen Clinical Trial Supply Prozesse und Lieferketten Vertretung des Bereichs Clinical Trial Supply (CTS) gegenüber relevanten internen und extern Stakeholder und Unterstützung der Abteilungsleitung

are searching for a Clinical Study Lead / Trial Manager to be responsible for all day-to-day CDO functional activities associated with the execution of a clinical study. In the case of a global, multi-country study, the

, burden of illness studies, external control arms to support single arm trials, and drive the development, analysis, and interpretation of patient-reported outcome (PRO) endpoints in clinical trials • Conduct systematic

, burden of illness studies, external control arms to support single arm trials, and drive the development, analysis, and interpretation of patient-reported outcome (PRO) endpoints in clinical trials • Conduct systematic

finalizing commercial terms and legal contracts with clients. Qualifications: Sales experience Commercial acumen Clinical trial services experience required Healthcare and pharmaceutical logistics knowledge What's on offer

. Thorough knowledge of International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical

improve compliances and processes • Working knowledge of clinical trial methodologies. • Excellent Benefits • Work-Life Balance • Growth and Development • Health and Wellbeing Support Daiichi Sankyo Europe GmbH

closely with the global HEOR Product Lead(s) and provides relevant input to ensure that clinical trials and global evidence generation programs deliver the data/evidence required for successful market access in the European

will lead the outsourced activities for conducting clinical trials. Some of your daily tasks will include: • Overseeing the planning and management of clinical trials, including selection and supervision of CROs

will lead the outsourced activities for conducting clinical trials. Some of your daily tasks will include: • Overseeing the planning and management of clinical trials, including selection and supervision of CROs

experience in a drug / biologic developing company, ideally in oncology indication or as clinical investigator in industry sponsored trials • Ability to work in a hierarchically flat, matrix environment • Strong working

project teams, as appropriate · Gather and disseminate competitive intelligence from multiple sources Core Competencies: · Must have an understanding of the clinical trial process, preferably deep understanding of executing

is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory

media screening for own and competitor brands, using innovative tools • Classify medical-scientific publications and clinical trial information • In collaboration with Insights Director, co-manage cross-functional CI

molecule product candidates are in various stages of clinical development. For more information, please visit: www.imux.com . This is a key and critical role within our organization and this should be reflected in the

molecule product candidates are in various stages of clinical development. For more information, please visit: www.imux.com . This is a key and critical role within our organization and this should be reflected in the

is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory

is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory