Clinical Research Coordinator 2

Tasso • Seattle, WA

3d • $75,000 - $90,000 • Onsite

About The Position

Tasso is a fast-growing Seattle-based startup focused on delivering at-home diagnostic testing to those who need it most. We are looking for a Clinical Research Coordinator 2, a Seattle-based role responsible for handling clinical research study materials and specimens for the Clinical team. This position will report to our Associate Director, Clinical Operations. An ideal candidate will have at a minimum 2 years’ experience in a participant-facing clinical research setting.

Requirements

• Authorized to work in the United States
• Primarily on-site in Seattle five days per week
• Bachelor’s Degree in a biological or health science field
• At least two years of experience in a clinical research coordinator or comparable role
• Medical Assistant Phlebotomist certification for Washington State, or readiness to obtain it
• Working knowledge of medical terminology, clinical trials, and Good Clinical Practice (GCP)
• Comfort working with clinical/laboratory data and research data systems; experience with EDC platforms preferred
• Proficiency with Microsoft Office and willingness to learn other research systems, e.g., EDC.
• Strong attention to detail, organizational skills, and the ability to manage multiple tasks across concurrent programs
• Ability to work both independently and as part of a distributed team
• Proficiency with Microsoft Office and willingness to learn research inventory and data systems
• GCP and IATA training (to be completed within 30 days of hire if not already held)

Nice To Haves

• Phlebotomy certification preferred (to be completed within 30 days of hire if not already held)

Responsibilities

• Recruit, prescreen, and obtain informed consent from prospective study participants
• Conduct clinical study visits, including collecting medical history, performing protocol-specified procedures and phlebotomy, and recording source data
• Provide study devices to participants and educate them on proper use
• Collect, process, and prepare specimens in accordance with clinical and laboratory protocols
• Maintain screening logs, enrollment logs, and participant records, both manually and electronically
• Enter and validate study data, e.g., into electronic data capture (EDC) platforms or study spreadsheets
• Support protocol compliance and participate in quality reviews of study activities
• Travel to partner laboratories, at-home collection sites, and additional clinic locations to support enrollment and data collection
• Support clinical and laboratory data cleaning, reconciliation, and query resolution across active studies, in partnership with the study team
• Assist with data listings, discrepancy review, and routine EDC data management tasks
• Maintain regulatory and essential documents and support Study Master File (SMF) upkeep
• Assist with study start-up and close-out activities and associated documentation
• Able to lift and handle laboratory shipments and supplies as needed
• Able to perform other responsibilities as assigned

Benefits

• $75K/yr - $90K/yr base salary + Stock Options
• 95% paid Medical, 100% Dental & Vision for employees and a generous subsidy for dependents
• 11 Paid Holidays and generous Time Off policies
• 401K + Employer Match
• Paid parental leave policy

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level