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Clinical Research Jobs in Bothell, WA (NOW HIRING)

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Clinical Research information

See Bothell, WA salary details

$54.8K

$120K

$211.3K

How much do clinical research jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical research in Bothell, WA is $119,990.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $136,900.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

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

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research jobs

What are the most commonly searched types of Clinical Research jobs in Bothell, WA?

The most popular types of Clinical Research jobs in Bothell, WA are:

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

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

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

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

Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Bothell, WA as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 23% Part Time, and 6% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $119,990 per year, or $57.7 per hour.

Clinical Research Assistant

Benaroya Research Institute

Seattle, WA • On-site

$22.55 - $31.35/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 1 day ago. 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 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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