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Clinical Research Data Abstractor Jobs in Renton, WA

Iterative Health

Clinical Research Coordinator II

Tacoma, WA · On-site

$26 - $34.75/hr

Clinical Research Coordinator II Iterative Health is a healthcare technology and services company ... Ensure all safety data is reviewed by the PI in a timely manner * Maintain inventory of study ...

Unavailable

Clinical Research Monitor II

Seattle, WA · Hybrid

$97.82K - $146.68K/yr

The Clinical Research Monitor partners closely with investigators, research coordinators, data managers, and regulatory staff to promote data integrity, participant safety, and continuous quality ...

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$20

$49

$70

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

As of May 31, 2026, the average hourly pay for clinical research data abstractor in Renton, WA is $49.64, according to ZipRecruiter salary data. Most workers in this role earn between $40.82 and $58.94 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Data Abstractor, and why are they important?

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 some 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 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 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 Renton, WA look for? The top searched job categories for Clinical Research Data Abstractor jobs in Renton, WA are:
What cities near Renton, WA are hiring for Clinical Research Data Abstractor jobs? Cities near Renton, WA with the most Clinical Research Data Abstractor job openings:
Clinical Research Data Abstractor jobs near you
Infographic showing various Clinical Research Data Abstractor job openings in Renton, WA as of May 2026, with employment types broken down into 2% As Needed, 82% Full Time, 12% Part Time, and 4% Contract. Highlights an 96% Physical, and 4% Hybrid job distribution, with an average salary of $103,256 per year, or $49.6 per hour.
Clinical Research Coordinator I

Clinical Research Coordinator I

Benaroya Research Institute

Seattle, WA • On-site

$25.66 - $37.21/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description

Overview
The Benaroya Research Institute (BRI) and Virginia Mason Medical Center (VMMC) seek a Clinical Research Coordinator (CRC) to join our Digestive Health Clinical Research team. The Center for Digestive Health at Virginia Mason is internationally known for bringing experts together to optimize care through innovations in research, education, and a multidisciplinary approach to treatment of digestive and liver diseases. Virginia Mason Franciscan Health was named by Healthgrades® as America's 100 Best Hospitals for Gastrointestinal Care.
The Clinical Research Coordinator I will oversee daily clinical trial operations, ensuring protocol compliance, coordinating patient visits, managing data, and facilitating communication among investigators, participants, and regulatory bodies. The ideal candidate will have a strong clinical research background, excellent organizational skills, and the ability to communicate complex information effectively. This role offers the opportunity to contribute to groundbreaking research aimed at improving treatments for digestive diseases alongside a team of dedicated experts.
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.
Responsibilities
  • Facilitate clinical research, including collaboration with affiliate or partnering research sites and conducting BRI-based studies
  • Prepare for new studies, including regulatory document filing and study monitor visit preparation
  • Screen and recruit study subjects, obtain informed consent, and document subject history
  • Review adverse events, concomitant medications, and ensure protocol compliance and subject safety
  • Handle test articles (TA), complete case report forms, and maintain source documents
  • Manage proper standard or research billing and ensure site quality
  • Coordinate subject care, including appointment scheduling, record reviews, treatment coordination, and health assessments
  • Collect vital signs, perform telephone triage/screening, and assist with subject arrivals
  • Conduct phlebotomy, specimen processing using universal precautions, and other procedures as appropriate
  • Participate in process improvement activities and develop corrective and preventive action plans

Qualifications
  • Minimum of one year full-time related experience required
  • Must maintain subject and document confidentiality at all times
  • Understand and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, IRB, and institutional policies and procedures
  • Requires good medical knowledge, including medical terminology and basic subject care
  • May require phlebotomy and vital sign collection skills, as well as the ability to operate centrifuges and EKG machines
  • Preferred: Higher education or vocational training specializing in healthcare
  • May require healthcare licensure or other specialized training

Compensation
$25.66 to $37.21 hourly
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 are powering possibility.To learn more, visit benaroyaresearch.org and connect with us on Facebook, Instagram, Threads, LinkedIn, Bluesky and 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 email jobs@benaroyaresearch.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

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