Site Activation Coordinator for Clinical Research (Calgary) …, Alberta

Become a Site Activation Coordinator, ensuring smooth operations and compliance in clinical studies from initiation to closure. Bring your expertise in study start-up to the forefront. As a Site Activation Coordinator, you will manage and support operational tasks for clinical studies effectively. This role involves preparing documents, coordinating activities with investigator sites, and ensuring adherence to regulatory requirements. Your previous experience in a pharmaceutical or CRO workplace will be critical as you facilitate timely communication and resolve issues efficiently throughout the study lifecycle. Key Responsibilities Coordinate site activation tasks and document management Manage regulatory submissions and approvals Interface between study teams and investigator sites Maintain clarity in study timelines and site readiness Conduct awareness sessions on compliance requirements Requirements Minimum 2 years' experience in study activation Solid knowledge of ICH, GCP, and FDA regulations Effective written and verbal communication skills Capable of operating multiple clinical systems Bachelor’s degree in a relevant field preferred Use your clinical trial expertise to excel as a Site Activation Coordinator and support successful research outcomes. #J-18808-Ljbffr Apply on Kit Job: kitjob.ca/job/2pkxvp