About the role

Premier Research is seeking a Site Start up Associate II to join our Clinical Monitoring, Site Management and SSU team in North Carolina. You will help ensure timely regulatory submissions and site start-up deliverables across global trials. You will coordinate with Project Managers, Clinical Leads, and Regulatory Start-up Managers, prepare local and central submissions, and review documents to ensure compliance with ICH/GCP and country-specific requirements.

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JOB OVERVIEW

Experience level

Senior

Location

Plymouth, NC

Occupation

Regulatory Affairs Specialists

Industry

Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Posted

today

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