Clinical Trial Coordinator – FSP

Job overview

The Clinical Trial Coordinator – FSP role is described as supporting work in the United States; the listing identifies Boise, ID, and compensation is not specified. The coordinator supports Parexel’s Clinical Research Manager and study team throughout the study lifecycle. The role helps maintain trial administration and documentation from start-up through closure. By coordinating site and regulatory materials, supplies, budgets, agreements, payments, and meetings, the coordinator contributes to compliant and timely study execution.

What you'll do

• Track essential documents and safety reports
• collate and distribute study tools
• update clinical trial databases and trackers
• coordinate clinical and non-clinical supplies and labeling
• prepare, distribute, and archive documents
• assist with electronic Trial Master File reconciliation and quality control
• support site start-up and regulatory submissions
• assist with budgets, agreements, payments, and financial compliance
• organize meetings
• complete required training and follow applicable procedures.

What we're looking for

Skills & competencies

clinical trial coordinator

fsp

clinical research

trial administration

document management

site start-up

regulatory support

etmf

budgets and payments

parexel

boise id

Work arrangement

• Weekend coverage required

Why this role

Clinical trial coordination role covering study administration, documentation, regulatory support, and budget-related processes.

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.