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Regulatory Affairs Study Start Up Specialist (level dependent on experience)

CTI Clinical Trial and Consulting • US • published 2026-10-01 03:58:50.061638

Description

**About CTI** CTI Clinical Trial and Consulting Services is a global, privately held, full\-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com (http://www.ctifacts.com) **Job Purpose/ Summary:** Manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB)Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with, assist and advise study teams, site personnel, sponsors, and CTI management to facilitate timely collection, assessment and processing of essential regulatory documentation and to provide ongoing status reports about the documentation. Maintain essential regulatory documentation for multiple studies and perform revie...

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