Clinical Trial Coordinator, Regulatory – FSP

Job overview

The Clinical Trial Coordinator, Regulatory – FSP role is described as supporting work in the United States; the listing identifies Boise, ID, and compensation is not specified. The coordinator supports the Clinical Research Manager and study team from study start-up through closure. The role helps keep trial documentation, regulatory submissions, site start-up, and related financial administration organized and compliant. Its coordination work supports timely study milestones and the accurate maintenance of trial records and processes.

What you'll do

• Track essential documents and safety reports
• collate and distribute study materials
• update trial databases and trackers
• coordinate supplies and labeling
• prepare, distribute, and archive clinical documents
• assist with electronic Trial Master File reconciliation and quality control
• support site evaluation, start-up, and regulatory submissions
• assist with budgets, agreements, payments, and financial procedures
• organize investigator meetings
• follow Parexel processes and applicable ICH-GCP requirements.

What we're looking for

Skills & competencies

clinical trial coordinator

regulatory

fsp

clinical research

trial documentation

site start-up

regulatory submissions

etmf

ich-gcp

parexel

boise id

Work arrangement

• Weekend coverage required

Why this role

Regulatory-focused coordinator role spanning trial documentation, site start-up, submissions, and study administration.

About the employer

Parexel is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.