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eTMF Spec I at CTI - ApplyBlast

eTMF Spec I

CTI

2 days ago

4.2 on Glassdoor

Lisboa, Portugal

Onsite

Full Time

Medior

0 applicants

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About this role

The eTMF Spec I role oversees and guides electronic Trial Master File processes, ensuring compliance, inspection readiness, and accurate documentation throughout clinical trials. The position involves monitoring trial progress, conducting quality control reviews, and collaborating with various clinical and regulatory teams to resolve documentation issues. The role also includes participating in audits, providing status reports, and supporting system enhancements to improve document management workflows.

Responsibilities

Oversee eTMF processes and ensure trial documentation compliance
Conduct quality control reviews of essential trial documents
Collaborate with cross-functional teams to resolve documentation issues

Skills

Qualifications

Bachelor's degree in allied health field such as nursing, pharmacy, or health science

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.