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

ist bereits in der finalen Phase III der klinischen Prüfung. Wir sind davon überzeugt, innerhalb der nächsten 24 Monate die erste Innovation in der Schmerzmitteltherapie seit mehr als 30 Jahren auf den Markt zu bringen. Unser Ziel

), Clinical Research Associates (CRAs), and Clinical Trial Associates (CTCs). Responsibilities include managing site and vendor matters in collaboration with Clinical Program Managers, under the supervision of the Assoc

, 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

experience in the pharmaceutical or CRO industry, specifically in clinical trials programming. Proven lead experience at the study-level, with a preference for candidates with prior exposure in Oncology Therapeutic Areas (TA

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

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

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

Scientist, Laboratory Technical Director, Chief Scientific Officer, Research and Development Manager, Clinical Trials Manager, Bioinformatics Scientist, Genomics Scientist, Pharmacology Director Industries:  Healthcare, Scientific

Scientist, Laboratory Technical Director, Chief Scientific Officer, Research and Development Manager, Clinical Trials Manager, Bioinformatics Scientist, Genomics Scientist, Pharmacology Director Industries:  Healthcare, Scientific

management systems for our clinical trials. You'll ensure compliance with industry standards and regulatory guidelines, manage external vendors, and collaborate with cross-functional teams to facilitate seamless data collection and

management systems for our clinical trials. You'll ensure compliance with industry standards and regulatory guidelines, manage external vendors, and collaborate with cross-functional teams to facilitate seamless data collection and

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