Seattle Clinical Research Center
Clinical Research Assistant
Seattle, Washington, US
Role snapshot
Seattle Clinical Research Center is hiring a Clinical Research Assistant on a full-time basis. This is an on-site role based in Seattle, Washington, US.
- Company
- Seattle Clinical Research Center
- Location
- Seattle, Washington, US
- Work mode
- On-site
- Job type
- Full-time
- Experience
- 1+ years
- Posted
- Nov 6, 2026
Who this role suits
People with roughly one to three years of experience who can own small pieces of work with light guidance and want to widen their scope.
How to prepare your application
- Prepare two or three stories about work you owned end to end, including one thing that went wrong and what you changed.
- Read what Seattle Clinical Research Center publishes about its product or team, so you can say clearly why this role and this company.
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About the role
The Research Assistant provides support to Clinical Research Coordinators in daily activities and procedures. Job specifics will vary depending on the area to which an RA is assigned, as well as previous experience in clinical research. An RA may be assigned to work exclusively with one coordinator or may also be assigned to multiple coordinators. There is a constant fluctuation of tasks and workload, which is directly related to the status of each study. There is little to no room for remote work in this position.
Essential Job Functions include, but are not limited to:
• Knowledge of GCP, HRP, ICH
• Understanding relationship between site, PI, sponsor, FDA, IRB and CRO
• Assist with scheduling subject visits
• Recruit/screen prospective study participants
• Complete EDC data entry
• Resolve EDC queries (basic)
• Process & ship labs in accordance with IATA guidelines
• Cleaning and restocking exam rooms
• Assist CRCs with maintaining study logs as needed
• ISF Filing
• Preparing patient charts for visits, including screening packets
• Preparation for monitoring visits (resolve all queries, ensure filing completed, pull charts)
• Unpacking/packing, storing, maintaining study supplies
• Complete study phone calls
• Review subject eDiary data for completion and re-education
• Labeling and copying IP (as directed by CRC)
• Sending and receiving record requests
• Assisting with medical record review
• Filing lab results
• Collecting patient vitals as needed
• Complete interim visits with patients as appropriate
• Assist with additional clinical procedures such as phlebotomy, electrocardiograms, etc. as appropriate
• Assist with archiving closed studies if needed
• Any other tasks listed on “Regulatory, CRC & RA Roles” document
In order to be eligible for this position, you should:
• Have excellent written and verbal communication skills
• Be detail oriented, organized, flexible, and willing to step in where needed
• Have at least 1 year experience in a healthcare setting
• Adhere to SCRC’s core values: Compassionate Care, Passion to Excel, Trust, Respect, and Collaborative Spirit
Pay Range: $26-$31 per hour.
Location: On-site