Clinical Research Associate II

Job overview

Clinical Research Associate II is an onsite role in Emeryville, CA. Compensation is not specified. The role supports clinical study teams and investigative sites through monitoring, site education, and oversight of data quality and patient safety. The associate manages assigned sites and monitoring activities in accordance with ICH-GCP guidelines, local regulations, and applicable standard operating procedures. This work supports compliant study execution and timely clinical trial milestones.

What you'll do

• Conduct site visits and prepare required documentation
• assess protocol and regulatory compliance
• build relationships with investigative sites and vendors
• provide study training
• track enrollment, case report form data entry, protocol deviations, and site issues
• communicate site performance to the Clinical Study Team
• mentor less experienced CRAs
• reconcile serious adverse events and resolve discrepancies
• support study milestones, audit preparation, and resolution of quality findings.

What we're looking for

Skills & competencies

clinical research associate ii

beone medicines

emeryville ca

onsite

clinical monitoring

clinical trials

site management

ich-gcp

patient safety

data quality

site visits

up to 70% travel

Work arrangement

• Weekend coverage required

Why this role

Up to 70% travel. Requires a relevant bachelor's degree, at least two years of clinical operations experience, and at least one year of monitoring experience. Global oncology trial experience is preferred.

About the employer

BeOne Medicines is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.