Manage remote site initiation with all clinical sites based on CURE51’s SOPs

Monitor the study and supervise the data upload process by study coordinators and PIs from all sites

Meet with the centers’ clinical teams to discuss the study, its results, any obstacles/issues they are facing and help them with solving them

Close sites and review data completion of each participating clinical team

Coordinate samples biobank collection and shipping to CURE51 Central Lab in Paris with CURE51 ops teams

Bachelor or Master Degree in a life sciences science/medicine related field

4-5 years of experience as a CRA in a multicentric and multicountry observational or interventional study

Proven ability to manage multiple tasks and projects simultaneously with a strong emphasis on organization and time management

Acute sense of operational details monitoring and ability to detect early signals and anomalies to alert and notify stakeholders about risk exposure

Excellent communication skills, capable of effectively coordinating with team members and reporting on project status

Experience in creating and implementing processes that increase efficiency in managing project timelines and deliverables

Fluent in French and English. German and/or Spanish is a bonus