... experience in project management of clinical trials. Fluent in Czech and English – oral and written. Understanding of clinical trial regulations in the Czech Republic. Excellent knowledge of clinical trial methodology. Up to date knowledge ...
... experience in project management of clinical trials. Fluent in Czech and English – oral and written. Understanding of clinical trial regulations in the Czech Republic. Excellent knowledge of clinical trial methodology. Up to date knowledge ...
... from site selection to post clinical trial activities. You will develop and execute specific TA trial delivery strategy, including trial:specific risk management plan. You ...
... experience in project management of clinical trials. Fluent in Czech and English – oral and written. Understanding of clinical trial regulations in the Czech Republic. Excellent knowledge of clinical trial methodology. Up to date knowledge ...
... processes and relevant experience as clinical trial investigator, or sub:investigator is ...
... and liaises with Clinical Research Managers (CRMs), Clinical Research Associates (CRAs) and Clinical Trial Coordinators (CTCs), Finance and Legal ... :Executes and oversees clinical trial country submissions and approvals for ...
... early planning phase for Sanofi’s clinical trials. You will be accountable for the clinical trial delivery (across studies) and implementation ... knowledgeable in Investigator site management, clinical trial operations, study development, regulations and ...
... to ensure completion of the Clinical Study Report. Set up and maintain the Trial Master File (TMF), Clinical Trial Management System (CTMS), and other ...
... in:quality TA:specific clinical trials through effective management of team to reach CDC CZ trial targets, incl. risk management. : Building ... years of experience in clinical trial management (including working as a Clinical Research Associate), with min 2 ...
... in-quality TA-specific clinical trials through effective management of team to reach CDC CZ trial targets, incl. risk management. Building ... 4 years of experience in clinical trial management (including working as a Clinical Research Associate), with min 2 ...