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Regulatory Affairs SSU at CTI - ApplyBlast

Regulatory Affairs SSU

CTI

3 months ago

4.2 on Glassdoor

Sydney, New South Wales, Australia

Onsite

Full Time

Medior

0 applicants

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About this role

The role supports clinical study start‑up by advising project teams on regulatory requirements, performing compliance assessments, preparing and reviewing regulatory submissions, and managing documentation quality. It involves interaction with sites, sponsors, and regulatory bodies to ensure adherence to country‑specific regulations and internal SOPs.

Responsibilities

Assist and advise project teams on regulatory requirements for clinical studies
Prepare, review, and submit regulatory documentation to IRBs and other authorities
Provide status reports and manage regulatory documentation throughout study start‑up

Skills

Qualifications

Associate’s Degree in allied healthBachelor’s Degree in allied health

About CTI

cti.com

Headquarters

Maryland Heights, Missouri, United States

Company Size

501-1000 employees

Founded

1988

View Profile

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.