Clinical Research Coordinator I
Tasso
Seattle, WA, USA
USD 26-34 / hour + Equity
Posted on Jun 2, 2025
Who We Are
Tasso is a fast-growing Seattle-based startup focused on delivering at-home diagnostic testing to those who need it most. We are growing our footprint with leading health systems, clinical research organizations, academic medical centers, and more who are looking to deliver clinical-grade, convenient diagnostic tests to their patients. Tasso was originally founded to find a better way to collect blood instead of a painful fingerstick or time-consuming venous draw. Since then, our products have been used in pharmaceutical clinical trials, by Olympians as part of a new virtual anti-doping program, and broadly by hospital systems across the US.
What You Will Do
Duties and tasks:
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Tasso is a fast-growing Seattle-based startup focused on delivering at-home diagnostic testing to those who need it most. We are growing our footprint with leading health systems, clinical research organizations, academic medical centers, and more who are looking to deliver clinical-grade, convenient diagnostic tests to their patients. Tasso was originally founded to find a better way to collect blood instead of a painful fingerstick or time-consuming venous draw. Since then, our products have been used in pharmaceutical clinical trials, by Olympians as part of a new virtual anti-doping program, and broadly by hospital systems across the US.
What You Will Do
Duties and tasks:
- Recruit, prescreen, and obtain informed consent from prospective study participants
- Conduct clinical study visits, including collecting medical history, performing protocol-specified procedures, and recording source data
- Support study visit logistics, including scheduling participants and maintaining enrollment and screening logs
- Perform general administrative tasks such as study preparation and maintenance of the Study Master File
- Collect, process, and store blood samples in accordance with clinical and laboratory protocols (e.g., centrifugation, aliquoting, storage)
- Package and ship clinical specimens according to protocol and regulatory requirements
- Enter and validate study data in clinical trial management systems, electronic data capture (EDC) platforms, or study spreadsheets
- Track and maintain inventory of clinic and laboratory supplies
- Prepare accessioning documents and shipping manifests for sample tracking
- Assist with collection, review, and tracking of essential regulatory documents (e.g., IRB approvals, informed consent forms, CVs, and licensure)
- Perform other duties as assigned
- Required Qualifications:
- Ability to be flexible, organized, and detail-oriented
- Licensed phlebotomist (or willingness to become licensed within 2 months of starting)
- Must be proficient in Microsoft Office, Word, and Excel, and databases used in research environment, and have a willingness to learn and demonstrate proficiency with new systems within 3 months of hire
- Associate's degree
- Able to be in office 5 days a week (Lower Queen Anne)
- Preferred Qualifications
- Bachelor's degree
- Good Clinical Practice (GCP) certification
- 100% paid Medical, Dental & Vision for employees and generous subsidy for dependents
- 11 Paid Holidays and generous Time Off policies
- 401K + Employer Match
- Paid parental leave policy
$26-34/hr + Stock Options
We offer competitive compensation, benefits and a fantastic work environment:
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