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Regulatory Affairs SSU at CTI - ApplyBlast

Regulatory Affairs SSU

CTI

26 days ago

4.2 on Glassdoor

Covington, Kentucky, United States

Onsite

Full Time

Medior

0 applicants

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About this role

This role manages essential regulatory documentation for clinical studies, ensuring timely submission to Institutional Review Boards, Ethics Committees, and Competent Authorities globally. The position involves advising study teams, reviewing and adapting study-specific documents, and maintaining accurate regulatory records throughout the trial lifecycle. It requires close collaboration with sponsors, site personnel, and project managers to facilitate compliance and documentation quality.

Responsibilities

Manage essential regulatory documentation for global clinical studies
Perform compliance assessments and IRB/EC submissions on behalf of sponsors
Review and adapt study-specific documents according to country requirements

Skills

Qualifications

Associate’s degree in allied health fieldBachelor’s degree in allied health field

About CTI

cti.com

Headquarters

Maryland Heights, Missouri, United States

Company Size

501-1000 employees

Founded

1988

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CTI (Conference Technologies Inc.) is a custom audio‑visual integrator that designs, installs, and supports AV systems and event productions. They serve corporate offices, houses of worship, and live events—building conference rooms, boardrooms, headquarters AV, video walls, and immersive meeting spaces. CTI provides end‑to‑end services from system design and integration to installation and ongoing support, aiming to connect people through technology and elevate audiovisual experiences.