Clinical Research Assistant — Hands-On Trials & Data

Benaroya Research Institute at Virginia Mason; Seattle (WA); On-site; USD 31,000 - 43,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

403(b) retirement plan

Paid time off

Educational assistance

Transit benefits

Job summary

Benaroya Research Institute at Virginia Mason is seeking a Clinical Research Assistant to support clinical research activities within the Clinical Research Program. You will work with Clinical Research Coordinators, investigators, and clinical staff to ensure study activities are performed accurately, efficiently, and per protocols and regulations.

The role involves study start-up, participant screening and recruitment, informed consent, data collection, regulatory documentation, specimen

Qualifications

• Knowledge of medical terminology and basic patient care.
• Strong organizational and attention-to-detail skills.
• Ability to follow protocols and procedures.

Responsibilities

• Support Clinical Research Coordinators with study activities.
• Assist with study start-up and preparation.
• Support participant screening, recruitment, and scheduling.
• Assist with informed consent activities.
• Collect participant history and protocol-required information.
• Document adverse events and concomitant medications.
• Support protocol-required participant visits and assessments.
• Obtain vital signs and perform basic health assessments.
• Coordinate participant appointments, treatments, and follow-up.

Skills

Medical terminology

Attention to detail

Protocol adherence

Communication

Team collaboration

Education

Medical Assistant license

Phlebotomist license

Medical Assistant–Registered

Tools

EMR systems

Research databases

Job description

Benaroya Research Institute at Virginia Mason is seeking a Clinical Research Assistant to support clinical research activities within the Clinical Research Program. You will work with Clinical Research Coordinators, investigators, and clinical staff to ensure study activities are performed accurately, efficiently, and per protocols and regulations.

The role involves study start-up, participant screening and recruitment, informed consent, data collection, regulatory documentation, specimen