Clinical Research Jobs in Washington
Clinical Research jobs in Washington are in strong demand, concentrated in biotechnology, academic medical research, and health systems, with openings ranging from entry-level research coordinator roles through senior principal investigators and clinical operations directors. Seattle, Bellevue, and Tacoma anchor most of the hiring, where employers like Fred Hutchinson Cancer Center, University of Washington Medicine, and Seattle Children's Research Institute maintain large, ongoing clinical trial programs. The most in-demand specialties include oncology trials, regulatory affairs coordination, and Phase II through IV study management. Find a role that fits below and apply directly.
Find Clinical Research JobsOverview
Showing 5 of 31+ Clinical Research jobs
The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC II will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES
1. Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
2. Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- a. Sponsor-provided and IRB-approved Protocol Training
- b. All relevant Protocol Amendments Training
- c. Any study-specific Manuals Training, as applicable
- d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
3. Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
4. Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
5. Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
6. Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
7. Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
8. Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
9. Demonstrating adherence and compliance to the assigned protocols at their respective site(s).
10. Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
11. Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
12. Demonstrating visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
13. Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
14. Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
15. Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
16. Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
17. Being prepared for and available at all required company meetings.
18. Submitting required administrative paperwork per company timelines.
19. Occasionally attending out-of-town Investigator Meetings
20. Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
21. Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
22. Facilitate effective communication between patients, healthcare providers, and research staff
23. Any other matters as assigned by management.
KNOWLEDGE & EXPERIENCE
Education:
- High School Diploma or equivalent required; Bachelor's degree preferred
- Foreign Medical Graduates preferred
Experience:
- At least 2 years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
Credentials:
- ACRP or equivalent certification is preferred
Knowledge and Skills:
- Be an energetic, go-getter who is detail-oriented and can multi-task.
- Be goals-driven while continuously maintaining quality.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC II will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES
1. Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
2. Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- a. Sponsor-provided and IRB-approved Protocol Training
- b. All relevant Protocol Amendments Training
- c. Any study-specific Manuals Training, as applicable
- d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
3. Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
4. Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
5. Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
6. Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
7. Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
8. Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
9. Demonstrating adherence and compliance to the assigned protocols at their respective site(s).
10. Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
11. Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
12. Demonstrating visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
13. Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
14. Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
15. Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
16. Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
17. Being prepared for and available at all required company meetings.
18. Submitting required administrative paperwork per company timelines.
19. Occasionally attending out-of-town Investigator Meetings
20. Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
21. Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
22. Facilitate effective communication between patients, healthcare providers, and research staff
23. Any other matters as assigned by management.
KNOWLEDGE & EXPERIENCE
Education:
- High School Diploma or equivalent required; Bachelor's degree preferred
- Foreign Medical Graduates preferred
Experience:
- At least 2 years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
Credentials:
- ACRP or equivalent certification is preferred
Knowledge and Skills:
- Be an energetic, go-getter who is detail-oriented and can multi-task.
- Be goals-driven while continuously maintaining quality.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
See All 31 Clinical Research Jobs in Washington
Find roles in Washington that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Washington
Where Washington roles are concentrated, by current openings.
Clinical Research Job Market in Washington
A snapshot from current Washington openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Non-Profit & Social Services
- Healthcare & Medical Services
What Washington Employers Look For
The qualifications that appear most often in clinical research jobs across Washington.
- ACRP or SOCRA certification (CCRC, CCRP) preferred or required by most Washington employers
- Bachelor's degree in life sciences, nursing, public health, or a related clinical field
- Experience with FDA regulations, GCP guidelines, and IRB submission processes
- Proficiency in electronic data capture systems such as Medidata Rave or REDCap
- Strong understanding of informed consent procedures and protocol compliance monitoring
- Ability to coordinate across multidisciplinary teams including principal investigators and sponsors
Clinical Research Jobs in Washington: Frequently Asked Questions
How do you become a clinical research in Washington?
Most clinical research positions in Washington require at minimum a bachelor's degree in a life science, nursing, or public health field, followed by hands-on trial experience. Washington does not issue a state license specific to clinical research coordinators, but employers strongly prefer candidates who hold a nationally recognized credential through the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA). University of Washington and Fred Hutchinson programs are common entry points.
Which companies hire clinical researchs in Washington?
Employers hiring clinical researchs in Washington right now include Fred Hutchinson Cancer Center, EmVenio Research, and Science 37, based on current listings on Migrate Mate as of August 2026. Washington's concentration of academic medical centers and biotech firms means clinical research hiring here tends to be tied to active trial portfolios rather than short-term contract surges.
Which Washington cities have the most clinical research jobs?
Seattle, Redmond, and Washington State account for the largest share of clinical research openings in Washington. Seattle drives the majority of listings due to its dense cluster of academic medical centers, biotech firms, and cancer research institutions, while Bellevue and Tacoma generate additional volume through regional health system satellite campuses and contract research organizations serving the greater Puget Sound area.
Are there remote clinical research jobs in Washington?
Yes, but they're limited. Clinical research work is largely site-based because trial monitoring, patient interaction, and regulatory oversight require physical presence. About 50% of clinical research openings tied to Washington are remote or hybrid as of August 2026, and those positions tend to cluster in regulatory affairs, data management, and sponsor-side monitoring roles rather than on-site coordination.
How can I get hired as a clinical research in Washington with little or no experience?
The most realistic entry path is a research coordinator or clinical trials assistant role at an academic medical center. University of Washington Medical Center and Seattle Children's Research Institute both post entry-level coordinator openings that accept candidates with a relevant bachelor's degree and no prior trial experience. Completing a Good Clinical Practice training course and volunteering in a campus research lab strengthens an application. Candidates transitioning from medical assisting, pharmacy technician, or clinical data entry roles are frequently considered for these positions.
Where can I find and apply to clinical research jobs in Washington?
You can find and apply to clinical research jobs in Washington directly on Migrate Mate, which lists current openings across the state. Search the available roles, identify the ones that match your experience and specialty area, and apply directly to each position that fits.
See All 31 Clinical Research Jobs in Washington
Find roles in Washington that match your experience and apply in just a few clicks.
Find Clinical Research Jobs