Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, youll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions:• Perform site monitoring
Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, youll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies
IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your
IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description We are looking for a Clinical Research Associate I (CRA I) to join our clinical operations team in Italy. As a CRA I, you will perform and coordinate clinical
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation What Youll Do Clinical Trial & Documentation Support Coordinate and complete assigned clinical trial