Site Activation Coordinator Clinical Research (Alberta)

Advance your career as a Site Activation Coordinator, where your study start-up expertise will ensure compliance and smooth operations in clinical research. Manage critical tasks for clinical studies from initiation to closure. In this role, your main focus will be on coordinating site activation and managing essential documents. You'll work closely with investigator sites, ensuring timely communication and adherence to regulatory requirements. Your background in a pharmaceutical or CRO setting will enhance your ability to address issues quickly throughout the study lifecycle. Key Responsibilities: • Coordinate site activation tasks and manage documentation • Handle regulatory submissions and approvals efficiently • Interface between study teams and investigator sites effectively • Maintain clarity in site readiness and study timelines • Conduct sessions on compliance requirements Requirements: • 2+ years' experience in study activation • In-depth knowledge of ICH, GCP, and FDA regulations • Solid written and verbal communication skills • Proficient with multiple clinical systems • Bachelor's degree in a relevant field preferred Utilize your clinical trial knowledge to excel in this crucial role for research success. #J-18808-Ljbffr Apply on Kit Job: kitjob.ca/job/2pkomh