Clinical Research Coordinator Jobs in Seattle, WA
Clinical Research Coordinator jobs in Seattle are in strong demand, concentrated in South Lake Union, First Hill, and the University District across academic medical centers, life sciences, and oncology research. Top employers hiring right now include Fred Hutchinson Cancer Center, Arcetyp, and Seattle Women's. Scan the live roles below and apply to whichever ones fit.
Find JobsOverview
Open roles15
Top employerFred Hutchinson Cancer Center
Work type71% On-site
Top credentialBachelor's degree
Companies hiring7
Showing 5 of 15+ Clinical Research Coordinator jobs
Clinical Research Coordinator II - NCTN
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Added 2d ago
Fred Hutchinson Cancer Center
Clinical Research Coordinator II - NCTN
Seattle, Washington
Added 2d ago
Clinical Research Coordinator II - Bilingual (Spanish)
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Added 2d ago
Seattle Children's
Clinical Research Coordinator II - Bilingual (Spanish)
Seattle, Washington
Added 2d ago
Clinical Research Coordinator III
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Added 5d ago
Fred Hutchinson Cancer Center
Clinical Research Coordinator III
Seattle, Washington
Added 5d ago
Clinical Research Coordinator I
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Added 1w ago
Fred Hutchinson Cancer Center
Clinical Research Coordinator I
Seattle, Washington
Added 1w ago
Clinical Research Data Coordinator -- Department of Medicine, Division of Hematology & Oncology
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Added 1w ago
University Of Washington
Clinical Research Data Coordinator -- Department of Medicine, Division of Hematology & Oncology
Seattle, Washington
Added 1w ago
Added 2d ago
Clinical Research Coordinator II - NCTN
Fred Hutchinson Cancer Center·Seattle, Washington
Job functions:
$32.63 - $48.93/hr
High school diploma or GED
1,001-5,000 employees
Job Description
Overview:
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
The Clinical Research Coordinator II is responsible for day-to-day coordination of National Clinical Trials Network (NCTN) clinical trials and associated research studies. The position oversees subject-level study workflows including screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research documentation. Collaborates with investigators, clinical teams, and Data Coordination staff within Clinical Research Support to ensure high-quality, compliant study conduct.
Reporting to the Senior Manager/Manager of Clinical Trials Coordination, the coordinator will be part of a centralized NCTN research team supporting clinical trial activities across multiple disease programs and care settings. This position serves as a shared departmental resource and may support study activation, enrollment, participant follow-up, and ongoing trial operations across Fred Hutch campuses and affiliated clinical sites.
This position is key to the successful conduct of NCTN studies and advancing clinical research efforts at Fred Hutch.
At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.
Responsibilities:
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
The Clinical Research Coordinator II is responsible for day-to-day coordination of National Clinical Trials Network (NCTN) clinical trials and associated research studies. The position oversees subject-level study workflows including screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research documentation. Collaborates with investigators, clinical teams, and Data Coordination staff within Clinical Research Support to ensure high-quality, compliant study conduct.
Reporting to the Senior Manager/Manager of Clinical Trials Coordination, the coordinator will be part of a centralized NCTN research team supporting clinical trial activities across multiple disease programs and care settings. This position serves as a shared departmental resource and may support study activation, enrollment, participant follow-up, and ongoing trial operations across Fred Hutch campuses and affiliated clinical sites.
This position is key to the successful conduct of NCTN studies and advancing clinical research efforts at Fred Hutch.
At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.
- Conduct daily clinical operations of assigned research studies in accordance with study protocols, regulatory and GCP guidelines, institutional policy, and applicable National Clinical Trials Network (NCTN) requirements.
- Develop and maintain tools for study implementation, including data collection tools, reference materials, and specific study orders; revise and utilize tools as necessary.
- Create and disseminate study-related educational content for internal and external audiences to ensure safe and accurate protocol implementation.
- Coordinate patient enrollment and participation by reviewing study candidates' medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.
- Schedule patient clinic visits and ongoing study visits; ensure administrative compliance with study protocols with respect to clinical procedures, laboratory tests, and other patient activities; may administer study questionnaires, ensure drug self-administration accountability with patients, and perform non-clinical ECGs.
- Support NCTN study activation, enrollment, conduct, and follow-up activities across multiple disease programs and clinical practice areas.
- Complete clinical requisition forms as instructed, assemble kits for patient visits, transport laboratory samples, and ensure samples are processed and shipped according to study guidelines; track and maintain research supplies.
- Identify, track, and confirm billable activities for patients; work with internal partners to obtain and submit budget and billing information; may assist in reviewing patient charges to ensure billing compliance.
- Act as protocol liaison with clinical teams, patients, providers, cooperative group representatives, and research staff on study-related topics.
- Prepare and coordinate monitoring visits and respond to queries and other requests from study monitors and cooperative groups, following up with and resolving any issues that may arise.
- Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, maintaining professional associations, and participating in cooperative group activities as applicable.
- Regularly travel between Fred Hutch campuses, affiliated clinical sites, and other research locations to support participant enrollment, study visits, research operations, protocol-specific activities, and attendance at investigator meetings.
- Assist with maintaining appropriate source documentation and/or performing case report form data entry.
- Serve as a shared departmental resource, providing flexible support across disease teams and clinical practice areas to facilitate NCTN study conduct, enrollment, and operational continuity.
- Demonstrate the ability to rapidly integrate into new disease programs, study portfolios, and clinical teams while maintaining high-quality study conduct and participant support.
- Other duties as assigned.
MINIMUM QUALIFICATIONS:
- High school diploma or equivalent.
- Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
- Knowledge of clinical trials records, procedures, and computerized data processing systems.
- Demonstrated knowledge of how to synthesize study conduct.
PREFERRED QUALIFICATIONS:
- Associate or bachelor’s degree preferred.
- Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA).
- Minimum five years of experience in a research environment with regulatory or human research protections.
- Previous experience working with NIH, FDA and OHRP regulations and medical terminology.
- Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
- Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
- Ability to work with multiple data management systems including generating reports and sourcing data from systems.
- Ability to extract data from medical records.
- Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.
The hourly pay range for this position is from $32.63 to $48.93 and pay offered will be based on experience and qualifications.
Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).
Additional Information: We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).
Fred Hutchinson Cancer Center
Clinical Research Coordinator II - NCTN
Seattle, Washington
Added 2d ago1,001-5,000 employees
Job functions:
$32.63 - $48.93/hr
High school diploma or GED
Job Description
Overview:
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
The Clinical Research Coordinator II is responsible for day-to-day coordination of National Clinical Trials Network (NCTN) clinical trials and associated research studies. The position oversees subject-level study workflows including screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research documentation. Collaborates with investigators, clinical teams, and Data Coordination staff within Clinical Research Support to ensure high-quality, compliant study conduct.
Reporting to the Senior Manager/Manager of Clinical Trials Coordination, the coordinator will be part of a centralized NCTN research team supporting clinical trial activities across multiple disease programs and care settings. This position serves as a shared departmental resource and may support study activation, enrollment, participant follow-up, and ongoing trial operations across Fred Hutch campuses and affiliated clinical sites.
This position is key to the successful conduct of NCTN studies and advancing clinical research efforts at Fred Hutch.
At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.
Responsibilities:
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
The Clinical Research Coordinator II is responsible for day-to-day coordination of National Clinical Trials Network (NCTN) clinical trials and associated research studies. The position oversees subject-level study workflows including screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research documentation. Collaborates with investigators, clinical teams, and Data Coordination staff within Clinical Research Support to ensure high-quality, compliant study conduct.
Reporting to the Senior Manager/Manager of Clinical Trials Coordination, the coordinator will be part of a centralized NCTN research team supporting clinical trial activities across multiple disease programs and care settings. This position serves as a shared departmental resource and may support study activation, enrollment, participant follow-up, and ongoing trial operations across Fred Hutch campuses and affiliated clinical sites.
This position is key to the successful conduct of NCTN studies and advancing clinical research efforts at Fred Hutch.
At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.
- Conduct daily clinical operations of assigned research studies in accordance with study protocols, regulatory and GCP guidelines, institutional policy, and applicable National Clinical Trials Network (NCTN) requirements.
- Develop and maintain tools for study implementation, including data collection tools, reference materials, and specific study orders; revise and utilize tools as necessary.
- Create and disseminate study-related educational content for internal and external audiences to ensure safe and accurate protocol implementation.
- Coordinate patient enrollment and participation by reviewing study candidates' medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.
- Schedule patient clinic visits and ongoing study visits; ensure administrative compliance with study protocols with respect to clinical procedures, laboratory tests, and other patient activities; may administer study questionnaires, ensure drug self-administration accountability with patients, and perform non-clinical ECGs.
- Support NCTN study activation, enrollment, conduct, and follow-up activities across multiple disease programs and clinical practice areas.
- Complete clinical requisition forms as instructed, assemble kits for patient visits, transport laboratory samples, and ensure samples are processed and shipped according to study guidelines; track and maintain research supplies.
- Identify, track, and confirm billable activities for patients; work with internal partners to obtain and submit budget and billing information; may assist in reviewing patient charges to ensure billing compliance.
- Act as protocol liaison with clinical teams, patients, providers, cooperative group representatives, and research staff on study-related topics.
- Prepare and coordinate monitoring visits and respond to queries and other requests from study monitors and cooperative groups, following up with and resolving any issues that may arise.
- Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, maintaining professional associations, and participating in cooperative group activities as applicable.
- Regularly travel between Fred Hutch campuses, affiliated clinical sites, and other research locations to support participant enrollment, study visits, research operations, protocol-specific activities, and attendance at investigator meetings.
- Assist with maintaining appropriate source documentation and/or performing case report form data entry.
- Serve as a shared departmental resource, providing flexible support across disease teams and clinical practice areas to facilitate NCTN study conduct, enrollment, and operational continuity.
- Demonstrate the ability to rapidly integrate into new disease programs, study portfolios, and clinical teams while maintaining high-quality study conduct and participant support.
- Other duties as assigned.
MINIMUM QUALIFICATIONS:
- High school diploma or equivalent.
- Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
- Knowledge of clinical trials records, procedures, and computerized data processing systems.
- Demonstrated knowledge of how to synthesize study conduct.
PREFERRED QUALIFICATIONS:
- Associate or bachelor’s degree preferred.
- Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA).
- Minimum five years of experience in a research environment with regulatory or human research protections.
- Previous experience working with NIH, FDA and OHRP regulations and medical terminology.
- Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
- Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
- Ability to work with multiple data management systems including generating reports and sourcing data from systems.
- Ability to extract data from medical records.
- Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.
The hourly pay range for this position is from $32.63 to $48.93 and pay offered will be based on experience and qualifications.
Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).
Additional Information: We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).
See All 15 Clinical Research Coordinator Jobs in Seattle
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Clinical Research Coordinator Jobs in Seattle: Frequently Asked Questions
How do I get a clinical research coordinator job in Seattle?
Focus your search on South Lake Union and First Hill, where Seattle's largest academic medical centers, cancer research institutes, and biotech companies cluster. Candidates with experience in oncology, immunology, or cardiovascular trials stand out in this market. Familiarity with electronic data capture systems and Good Clinical Practice certification gives you a concrete edge when applying to Seattle's research-heavy institutions.
Which companies hire clinical research coordinators in Seattle?
Employers hiring clinical research coordinators in Seattle right now include Fred Hutchinson Cancer Center, Arcetyp, and Seattle Women's, based on current listings on Migrate Mate as of November 2026. Seattle's hiring mix runs from large academic medical systems and NCI-designated cancer centers to mid-size biotech firms and contract research organizations embedded in the city's life sciences corridor.
Are there remote clinical research coordinator jobs in Seattle?
Yes, though with limits, since the role involves hands-on patient contact and site visits that require in-person presence for most positions. About 29% of clinical research coordinator openings tied to Seattle are remote or hybrid as of November 2026, with the remote-eligible work tending toward data entry, regulatory documentation, and sponsor communication rather than participant-facing duties.
How can I get a clinical research coordinator job in Seattle with little or no experience?
The most realistic entry path in Seattle is through a clinical research assistant or study coordinator internship at one of the city's academic medical centers or university-affiliated research programs in the University District. Volunteering for institutional review board support roles or gaining experience as a medical scribe at a Seattle clinic can also build the documentation and protocol familiarity that hiring managers look for in entry-level candidates.
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