CareerPlanSign in

Project Assistant

Austin, Texas, USA💼 Full-time🗓 2026-09-29

Core

Managing regulatory documents, facilitating IRB submissions, and ensuring audit-ready files for clinical studies.

Role type

Project Assistant (Clinical Research)

Domain

Clinical research / Regulatory affairs

Deliverable

client delivery

Required skills

Regulatory document management, IRB submission facilitation, audit preparation

Responsibilities

Managing study regulatory documents, facilitating IRB submissions, ensuring study training compliance, maintaining audit-ready files

Sourced via workday · Listed on CareerPlan, which tracks 853,000+ jobs from 20+ sources.