... ? Are you passionate about clinical research? If yes, you might be our new Clinical Operations Manager. This position is ... 4 years of experience in clinical trial management (including working as a Clinical Research Associate), with min 2 years of ...
... are currently seeking an Experienced Clinical Research Associate to join our Clinical Country Operations team in Prague. ...
... Institute is comprised of three research centres which build upon the ... Region for Biotechnological and Agricultural Research (CRH), the Regional Centre of ... the Czech Advanced Technology and Research Institute of Palacký University Olomouc ...
... studies, as well as other clinical services such as managed access programs, research collaborations, and digital solutions. Working ...
... a Senior CRA or Trial Manager background and have experience in managing the implementation of clinical systems and software solutions. As a Clinical System Implementation Manager, you will ... them. From research and development, through to manufacturing, ...
... timelines, budgets, and monitor progress to ensure adherence to deadlines and budgetary constraints. You conduct thorough assessments of current clinical processes and systems to identify ... them. From research and development, through to manufacturing, ...
... , timelines, budgets, and monitor progress to ensure adherence to deadlines and budgetary constraints.-Conduct thorough assessments of current clinical processes and systems to identify ... seize them. From research and development, through to manufacturing, ...
... timelines, budgets, and monitor progress to ensure adherence to deadlines and budgetary constraints. You conduct thorough assessments of current clinical processes and systems to identify ... them. From research and development, through to manufacturing, ...
... , timelines, budgets, and monitor progress to ensure adherence to deadlines and budgetary constraints. Conduct thorough assessments of current clinical processes and systems to identify ... seize them. From research and development, through to manufacturing, ...
... smooth study setup and conduct, monitor site performance, address protocol deviations, ... . Review site visit reports and monitor activities for quality control. Chip ... essential study documents. Contribute to clinical sections of regulatory documents and ...