Senior Clinical Research Associate

Job overview

The Senior Clinical Research Associate role is listed with a remote location in Oregon, but the posting describes onsite monitoring visits and does not specify a remote work arrangement. Compensation is not specified. PSI conducts clinical research projects across therapeutic areas and works to bring new medicines to patients. The role monitors clinical research sites and study activities to support project timelines, regulatory compliance, data quality, and the rights, safety, and well-being of study participants. It also coordinates with investigators, project stakeholders, vendors, and internal teams throughout study execution.

What you'll do

• Conduct and report onsite monitoring visits
• participate in study startup when applicable
• review case report forms, verify source documents, and resolve queries
• manage site communications
• supervise country-level study activities and timelines
• coordinate with support services and vendors
• participate in quality control and feasibility research
• support regulatory submission documents.

What we're looking for

Skills & competencies

senior clinical research associate

psi cro

clinical research

site monitoring

onsite monitoring visits

oncology trials

phase i–iii

source document verification

regulatory submissions

up to 80% travel

oregon listing

Work arrangement

• Weekend coverage required

Why this role

Requires at least five years of independent U.S. onsite monitoring experience and complex oncology trial monitoring experience. Travel may be up to 80%. The employer is not hiring applicants who require work visas now or in the future.

About the employer

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