Clinical Research Assistant
About The Position
The Clinical Research Assistant supports clinical research activities within the Clinical Research Program at Benaroya Research Institute (BRI). Working closely with Clinical Research Coordinators, investigators, and clinical staff, the Clinical Research Assistant assists with the conduct of clinical research studies and helps ensure that study activities are performed accurately, efficiently, and in accordance with study protocols and applicable regulations. The Clinical Research Assistant may support research conducted at BRI, as well as studies involving affiliate or collaborating research sites. Responsibilities may include study start-up and preparation, participant screening and recruitment, informed consent, clinical data collection, participant care coordination, regulatory documentation, test article handling, specimen collection and processing, and maintenance of accurate source documentation and case report forms. This position is an excellent opportunity for an individual interested in developing a career in clinical research while gaining hands-on experience with clinical trial operations, participant interaction, and research processes.
Requirements
- Knowledge of medical terminology and basic patient care.
- Strong organizational and attention-to-detail skills.
- Ability to follow protocols and procedures.
- Effective written and verbal communication skills.
- Ability to work collaboratively in a multidisciplinary team.
- Commitment to participant safety and research quality.
- Medical Assistant, Phlebotomist, and Medical Assistant–Registered licenses, or ability to obtain licensure after hire.
Nice To Haves
- Healthcare or vocational training in a related field.
- Experience in healthcare, clinical research, or patient care.
- Knowledge of clinical research practices and terminology.
- Familiarity with FDA, GCP, ICH, HIPAA, and IRB requirements.
- Experience with vital signs, phlebotomy, or specimen processing.
- Experience with electronic medical records or research databases.
- Interest in pursuing a career in clinical research.
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.
- Conduct telephone screening and triage as appropriate.
- Coordinate participant appointments, treatments, and follow-up.
- Communicate professionally with participants and research staff.
- Maintain accurate source documentation and study records.
- Assist with case report form completion.
- Enter and maintain clinical research data.
- File and maintain regulatory documents.
- Assist with preparation for monitoring visits and audits.
- Identify and escalate protocol or data issues.
- Support appropriate research and standard billing.
- Maintain participant and study confidentiality.
- Collect, process, label, and store research specimens.
- Perform phlebotomy as permitted by licensure and training.
- Handle test articles according to study requirements.
- Follow universal precautions and safety procedures.
- Follow study protocols and institutional procedures.
- Comply with FDA, GCP, ICH, HIPAA, and IRB requirements.
- Support participant safety and study quality.
- Maintain required training and competencies.
- Participate in quality and process improvement activities.
- Perform other duties as assigned.
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
