Job Summary: The Manager Clinical Study Lead (CSL) will be responsible for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out.
The CSL is accountable for the study timelines, budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP.}
This role involves leading cross-functional study teams, providing operational input into protocol development, overseeing and contributing to the development of study specific documentation, and managing study systems including CTMS and TMF.
The ideal candidate will have a minimum of a Bachelor's degree and 6+ years of direct clinical trial experience, with technical proficiency in trial management software and MS applications. They will also possess excellent interpersonal and leadership skills, with the ability to understand and implement operational strategic direction and guidance for respective clinical studies.