Research Assistant I/II

Benaroya Research Institute•Seattle, WA

4d•$24 - $34•Hybrid

About The Position

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.

Requirements

High school diploma required
Strong computer, organizational, written, and interpersonal skills
Ability to work under supervision and follow detailed protocols
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

Nice To Haves

Healthcare or clinical research experience preferred
Prior experience with regulatory or clinical study operations preferred

Responsibilities

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., OneNet 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
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