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$9

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$51

How much do clinical research assistant jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for clinical research assistant in Bothell, WA is $25.39, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $29.04 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
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What are the most commonly searched types of Clinical Research jobs in Bothell, WA?

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

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

Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Bothell, WA as of August 2026, with employment types broken down into 2% As Needed, 80% Full Time, 12% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $52,810 per year, or $25.4 per hour.

Clinical Research Assistant

Seattle, WA • On-site

Benaroya Research Institute
Scientific Research and Development Services • 201 - 500 employees
Learn more about Benaroya Research Instituteexternal

$22.55 - $31.35/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

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 hour 

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.

Employment Type: FULL_TIME

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