Clinical Research Coordinator I — Meaningful Trials & Growth

MultiCare Clinics; Tacoma (WA); On-site; USD 39,000 - 56,000; Full time

Job summary

MultiCare Clinics in Tacoma, WA seeks a Clinical Research Coordinator I to implement clinical studies, including basic science, phase II–IV trials, and IIR studies, coordinating with nursing staff, physicians, patients, and external partners.

The role includes handling study visits, data collection, specimen processing, and ensuring regulatory compliance, with a Day shift and FTE 1.0. A background in healthcare research and CPR is preferred, and a WA driver's license is required.

Qualifications

• High school education required.
• Bachelor’s degree in science, healthcare or related field preferred.
• Minimum 1 year of research assistant or coordinator experience in healthcare.
• CPR certification required.
• Valid Washington State driver’s license.

Responsibilities

• Coordinates clinical research pertaining to clinical research in human subjects.
• Follows guidelines for identifying subject populations, complete forms, questionnaires, and clinic procedures for collecting and summarizing observations and data.
• Prepares for and participates in study monitor visits.
• May perform venous blood draws within the practice scope of a Medical Assistant – Phlebotomy license.
• Coordinates and oversees processing, inventory and shipping of study specimens.
• Documents and maintains accurate records of study visits and procedures to include financial accrual, source document and eCRF completion in compliance with applicable regulations and department procedures.
• Completes and submits sponsor queries within 3 – 5 business days from receipt.

Skills

Clinical research coordination

Data collection

Subject recruitment

Education

High school diploma

Bachelor's degree in science/healthcare

Tools

CPR certification

Driver's license

Job description

MultiCare Clinics in Tacoma, WA seeks a Clinical Research Coordinator I to implement clinical studies, including basic science, phase II–IV trials, and IIR studies, coordinating with nursing staff, physicians, patients, and external partners.

The role includes handling study visits, data collection, specimen processing, and ensuring regulatory compliance, with a Day shift and FTE 1.0. A background in healthcare research and CPR is preferred, and a WA driver's license is required.