Clinical Trial Coordinator - FSP

Job overview

The Clinical Trial Coordinator - FSP position is explicitly remote and available anywhere in the United States. Compensation is not specified. The coordinator supports Parexel and client study teams throughout the study lifecycle, from start-up to closure. The role keeps trial administration, documentation, regulatory support, and related coordination organized across study teams. By maintaining trackers and records and assisting with site start-up and study processes, it helps the team meet clinical research requirements and move studies through completion.

What you'll do

• Track essential documents and safety reports
• distribute study tools and documents
• update clinical trial databases and trackers
• coordinate clinical and non-clinical supplies
• manage labeling and translation requests
• prepare, distribute, and archive documents
• assist with electronic Trial Master File reconciliation and quality control
• support site start-up, submissions, budgets, agreements, payments, and meetings.

What we're looking for

Skills & competencies

clinical trial coordinator

fsp

parexel

remote

united states

clinical research

trial administration

document management

regulatory support

site start-up

trial master file

ich-gcp

Work arrangement

• Weekend coverage required

Why this role

The posting states that the position is remote and can be performed anywhere in the United States.

About the employer

Parexel is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.