Location: Chicago, ILJob Description:Responsible for study start up activities and regulatory maintenance of assigned portfolio of clinical research studies.Creation and maintenance of study regulatory files in study binders, shared drives, and/or eRegulatory product.Prepares regulatory files for monitoring and auditing activities and addresses outstanding issues resulting from routine monitoring activities.Provides guidance to PIs, research team, auditors, and other affiliated staff related to the maintenance of regulatory compliance. Participates in working groups and/or other internal committees as assigned.Completes internal trainings as needed.Coordinates dep