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Clinical Research Data Abstractor Jobs in Bothell, WA

Enter and validate study data, e.g., into electronic data capture (EDC) platforms or study ... At least two years of experience in a clinical research coordinator or comparable role * Medical ...

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Clinical Research Data Abstractor information

See Bothell, WA salary details

$20

$49

$70

How much do clinical research data abstractor jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research data abstractor in Bothell, WA is $49.34, according to ZipRecruiter salary data. Most workers in this role earn between $40.58 and $58.56 per hour, depending on experience, location, and employer.

What is a clinical research data abstractor?

A Clinical Research Data Abstractor is a professional responsible for collecting and extracting important data from medical records, clinical trials, or patient charts. They ensure that the data is accurate, complete, and entered into research databases or electronic systems. This role is vital in supporting clinical research studies by ensuring high-quality data for analysis, compliance, and reporting. Clinical Research Data Abstractors often work closely with research coordinators, physicians, and other healthcare professionals.

What skills and qualifications are needed to be a clinical research data abstractor?

To thrive as a Clinical Research Data Abstractor, you need strong attention to detail, knowledge of medical terminology, and experience with data collection, often supported by a degree in health sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and possibly certifications like ACRP-CP or SoCRA-CCRP is common. Excellent organizational skills, critical thinking, and the ability to communicate clearly with research teams help set top performers apart. These skills ensure accurate, timely data abstraction that is vital for regulatory compliance and the integrity of clinical research studies.

What are common challenges faced by clinical research data abstractors, and how can they be managed?

Clinical Research Data Abstractors often encounter challenges such as interpreting complex medical records, ensuring data accuracy, and navigating various electronic health record (EHR) systems. To manage these challenges, it's helpful to develop strong attention to detail, maintain up-to-date knowledge of medical terminology, and collaborate closely with clinical teams for clarification when needed. Additionally, frequent communication with data managers and adhering to standardized data abstraction protocols can greatly reduce errors and improve data quality.

What is the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?

AspectClinical Research Data AbstractorClinical Research Coordinator
Primary RoleExtracts and summarizes data from clinical trial recordsManages overall study operations and participant coordination
Required SkillsAttention to detail, data management, basic medical knowledgeRegulatory compliance, patient interaction, study oversight
Work EnvironmentData entry labs, clinical trial sites, research officesClinical sites, hospitals, research institutions
CertificationsTypically none required, but certifications like CCR can helpOften requires CCRC or similar certifications

While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

What job categories do people searching Clinical Research Data Abstractor jobs in Bothell, WA look for?

The top searched job categories for Clinical Research Data Abstractor jobs in Bothell, WA are:

What cities near Bothell, WA are hiring for Clinical Research Data Abstractor jobs?

Cities near Bothell, WA with the most Clinical Research Data Abstractor job openings:

Infographic showing various Clinical Research Data Abstractor job openings in Bothell, WA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $102,619 per year, or $49.3 per hour.

Clinical Research Assistant

Benaroya Research Institute

Seattle, WA โ€ข On-site

$22.55 - $31.35/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Overview

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.

ResponsibilitiesClinical Research support
  • 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.
Research data and documentation
  • 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.
Specimen and Test Article support
  • 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.
Compliance and quality
  • 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.
QualificationsRequired
  • 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.
Preferred
  • 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.
Compensation

$22.55 to $31.35 per hourย 

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
About Us

The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to patients, giving them access to clinical trials for over 100 different conditions including cancer, digestive disease, cardiology, and neuroscience. The Clinical Research Program at BRI oversees all clinical research at Virginia Mason Medical Center, combining the expertise of a world-renowned research institute with remarkable healthcare to support studies that contribute to improving the diagnosis, treatment, and prevention of a variety of diseases.

BRI is an independent, nonprofit research institute affiliated with Virginia Mason Franciscan Health and based in Seattle. Our culture is based on the values of collaboration, respect, innovation, and inquiry; team members work together to support patients and clinicians with the goal of better outcomes for all.

At BRI, each role is valued and an important contributor to our vision and mission. BRI is committed to a safe, caring and diverse workplace; as well as to taking action to further our commitments to foster inclusion, equity and belonging so employees feel comfortable bringing their full selves to work. Consider making a difference by joining our team. Because together, we areย powering possibility.To learn more, visitย benaroyaresearch.orgย and connect with us onย Facebook,ย Instagram,ย Threads,ย ย LinkedIn,ย Blueskyย andย YouTube.Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. If you need an accommodation or assistance completing the online application, please contact Human Resources at 206-342-6547 or emailย jobs@benaroyaresearch.org.ย This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

Employment Type: FULL_TIME