Study Start Up Specialist II

A Clinical Site Activation Specialist at Parexel manages the start-up and maintenance phases of clinical trials, acting as the primary point of contact for investigation sites. The role involves coordinating regulatory submissions, preparing essential study documents like Informed Consent Forms, and ensuring sites are audit-ready through rigorous compliance monitoring. This position requires working independently to forecast activation plans, resolve site-level issues, and maintain high-quality data within Trial Management Systems.