Clinical Research Coordinator

Clinical Research Coordinator Overlake Arthritis & Osteoporosis Center - 4.0 Bellevue, WA Job Details Full-time $24 - $29 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Qualifications Biology Vital signs Clinical research Bachelor's degree in biology Bachelor's degree Clinical trials Full Job Description Clinical Research Coordinator | Rheumatology Research Job description: We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to join a growing rheumatology research program conducting industry-sponsored clinical trials. This is an excellent opportunity for a research professional who enjoys patient interaction, thrives in a fast-paced environment, and is passionate about advancing treatments for patients with rheumatic and autoimmune diseases. The ideal candidate is a quick learner, highly organized, detail-oriented, and experienced in coordinating clinical trials from study start-up through closeout. Candidates with experience using

CRIO, EDC

platforms, and other clinical research systems are strongly encouraged to apply.

The Clinical Research Coordinator will:

Coordinate clinical trial activities in accordance with study protocols, GCP guidelines, and regulatory requirements. Screen, recruit, and enroll eligible study participants. Obtain and document informed consent under investigator supervision. Schedule and coordinate study visits, procedures, and participant follow-up. Perform protocol-required procedures such as vital signs, ECGs, specimen collection, and patient questionnaires, as permitted by training and protocol. Collect, review, and enter study data into electronic data capture (EDC) systems. Maintain accurate source documentation, study binders, regulatory files, and participant records. Process, label, store, and ship laboratory specimens according to protocol requirements. Monitor participant compliance and maintain communication with study participants throughout the trial. Report adverse events and protocol deviations to investigators and assist with required documentation. Communicate with sponsors, CROs, laboratories, and study vendors regarding study-related activities. Prepare for sponsor monitoring visits, audits, and inspections. Maintain investigational product accountability and assist with study drug/device management. Assist with recruitment efforts and study outreach activities. Participate in team meetings, sponsor training, and continuing education activities. Ensure compliance with study protocols, institutional policies, and applicable federal regulations.

Bonus skills:

Thorough knowledge of CRIO and EDC.

Additional Requirements:

Bachelor's degree in biology Interest in continuing with research as a career path. Must be willing to commit to at least 2 years and have at least 1 year of clinical research experience in the US. Must have vaccinations in accordance with CDC guidelines in addition to completed COVID vaccination series.

Job Type:

Full-time Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance

Medical Specialty:

Rheumatology Application Question(s): Does the salary listed meet your expectations? This position is on-site, and you must live in WA state prior to accepting this position if offered. Do you reside in WA state?

Education:

Bachelor's (Required)

Experience:

Clinical research: 1 year (Required)

Work Location:

In person

Job Type:

Full-time Pay:

$24.00 - $29.00 per hour

Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance

Medical Specialty:

Rheumatology Application Question(s): Does the salary listed meet your expectations? This position is on-site, and you must live in WA state prior to accepting this position if offered. Do you reside in WA state?

Education:

Bachelor's (Required)

Experience:

Clinical research: 1 year (Required)

Work Location:

In person