Research Assistant I​/II

Overview

Benaroya Research Institute (BRI) and Virginia Mason Medical Center (VMMC) are leaders in conducting cancer clinical trials aimed at improving cancer treatment and prevention. Their studies encompass chemotherapy, radiation, targeted therapies, diagnostic test development, and quality of life/symptom management. Annually, over 100 cancer-related clinical studies are conducted, including those sponsored by the National Cancer Institute and industry partners. The Cancer Clinical Research Unit is actively engaged in various cancer research areas, with ongoing clinical research studies.

Hybrid work may be allowed occasionally depending on workload, research patient schedule, and job performance. The work schedule may vary - it is typically Monday through Friday from 8:00 AM to 4:30 PM, with a 30-minute lunch break.

Research Assistant I

• Provides administrative and operational support to Clinical Research Coordinators in the conduct of clinical research studies
• Assists with study start-up activities, regulatory file maintenance, and document management
• Supports scheduling of study participants, data entry, and maintenance of study databases and centralized repositories
• Assists with management of study supplies, lab kits, and secure document uploads (e.g., One Net or equivalent systems)
• May support clinical procedures such as vitals, EKGs, blood draws, sample processing, participant screening/recruitment, and study questionnaires under supervision
• Handles routine transport of investigational product as needed

Research Assistant II

• Performs all duties of Research Assistant I with increased independence and responsibility
• Supports study start‑up, regulatory documentation, and maintenance of research databases with reduced supervision
• Independently manages participant scheduling, data entry, and routine study coordination tasks
• Oversees accurate management of study documentation, lab kits, and secure data/image submissions
• May perform delegated clinical procedures (e.g., vitals, EKGs, blood draws, sample processing) and participant interactions per protocol
• Provides advanced support to coordinators and assists with study workflow coordination and problem‑solving

Research Assistant I

• High school diploma required
• Strong computer, organizational, written, and interpersonal skills
• Healthcare or clinical research experience preferred
• Ability to work under supervision and follow detailed protocols

Research Assistant II

• High school diploma required
• Minimum 9 months full‑time experience in clinical research or related healthcare/research role required
• Strong organizational, communication, computer, and interpersonal skills
• Demonstrated ability to work independently and reliably in a clinical research setting
• Prior experience with regulatory or clinical study operations preferred

Research Assistant I - $22.55 to $31.35 hourly

Research Assistant II - $24.05 to $34.15 hourly

• Medical, dental, vision insurance
• Flexible spending accounts: health care, dependent care, commuter
• Short and long-term disability
• Life and AD&D insurance
• 403(b) retirement plan with matching funds after one year of employment
• PTO: 13 holidays, three weeks of vacation and two weeks of sick leave per year
• Employee assistance program
• Educational assistance program
• Subsidized ORCA pass
• Wellness benefits
• Voluntary benefits

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status or any other characteristic protected by state or federal law.