Clinical Research Associate II (US West) - FSP

Job overview

The Clinical Research Associate II (US West) - FSP role is listed in Olympia, WA; the posting also identifies remote and on-site monitoring activities but does not specify a work arrangement. Compensation is not specified. The role supports clinical research studies by managing allocated study sites throughout trial phases. The associate serves as the primary site contact, overseeing monitoring, documentation, site readiness, and communication with investigators and site staff. The work helps ensure reliable study data, participant safety, and compliance with protocols, Good Clinical Practice, sponsor procedures, and applicable regulations.

What you'll do

• Manage site relationships and monitoring activities throughout trial phases
• conduct remote and on-site monitoring and oversight
• perform site visits and document visit and non-visit contacts
• review regulatory documentation
• communicate with investigators and site staff about study conduct and performance
• identify and resolve site quality or compliance issues
• maintain trial management and electronic trial master file records
• contribute to team knowledge and support audits or inspections as needed.

What we're looking for

Skills & competencies

clinical research associate ii

us west

fsp

olympia wa

parexel

clinical trials

site monitoring

good clinical practice

ich-gcp

regulatory documentation

investigator relations

trial master file

Work arrangement

• Weekend coverage required

Why this role

Requires a minimum of two years of direct site monitoring experience in bio/pharma/CRO. A bachelor's degree with a strong emphasis in science and/or biology is preferred.

About the employer

Parexel is hiring for this role. Industry: Process, Physical Distribution, and Logistics Consulting Services. Sector: 54.