Controlled Documents Specialist

Emmes Group: Building a better future for us all.

Overview

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Founded more than 47 years ago, Emmes has become one of the primary clinical research providers to the U.S. government before expanding into public‑private partnerships and commercial biopharma. We have built industry‑leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. Our mission is to have a direct impact on patients’ lives and to build a collaborative, performance‑driven culture.

Job Summary

The Controlled Documents Specialist is responsible for managing the controlled document lifecycle within the Veeva Quality platform, ensuring compliance with regulatory requirements, internal processes, and quality management standards.

Responsibilities

• Manag...