Senior Clinical Research Associate (FSP) — Dover, Dallas, San Francisco, or Jacksonville

Job overview

The Senior Clinical Research Associate (FSP) role is listed in Dallas, TX; San Francisco, CA; or Jacksonville, FL, while the feed’s primary location is Dover, DE. The listing does not specify compensation. Parexel supports pharmaceutical and biotechnology companies with clinical development services; the role requires travel of 55–75% as study needs dictate. The Senior Clinical Research Associate monitors and manages clinical trial sites from evaluation and initiation through monitoring and closeout. By checking site conduct, data, documentation, and regulatory compliance, the role helps clinical study teams maintain reliable trial execution and data validity.

What you'll do

• Apply study procedures and monitoring plans
• help identify investigators
• conduct pre-study, initiation, interim monitoring, and closeout visits
• train site staff
• review source data and essential documents
• monitor protocol, Good Clinical Practice, and IRB compliance
• track study progress and action items
• maintain the Clinical Trial Management System
• support issue resolution, audits, and data management as assigned.

What we're looking for

Skills & competencies

senior clinical research associate

fsp

clinical trial monitoring

dover de

dallas tx

san francisco ca

jacksonville fl

parexel

phase i trials

good clinical practice

source data review

clinical trial management system

oncology or immunology preferred

55–75% travel

Work arrangement

• Weekend coverage required

Why this role

Phase I clinical trial monitoring experience is required; oncology or immunology experience is preferred. Travel is 55–75%.

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.