Clinical Research Coordinator II — Drive Quality Trials

Dm Clinical Research Group; Seattle (WA); On-site; USD 68,000 - 85,000; Full time

Job summary

Dm Clinical Research Group in Seattle, WA seeks a Clinical Research Coordinator II to ensure quality studies per sponsor protocol, FDA regulations, and ICH/GCP guidelines.

You will oversee subject visits, data entry, and regulatory documentation, coordinate training, monitor enrollment, and liaise with investigators, lab, and sponsor teams to meet timelines. Strong communication, detail-orientation, multitasking, and 2+ years CRC experience preferred; bilingual English/Spanish preferred.

Qualifications

• High School Diploma or equivalent; Bachelor's degree preferred.
• At least 2 years of CRC experience.
• ACRP certification preferred.
• Proficient English; bilingual English/Spanish preferred.

Responsibilities

• Conduct study visits and document procedures per protocol.
• Maintain ALCOA-C compliant trial documentation.
• Perform data entry and resolve queries per sponsor guidelines.
• Ensure enrollment goals are met and communicate with sponsors.
• Coordinate training and ensure regulatory compliance.

Skills

Bilingual English/Spanish

Detail-oriented

Multitask

Strong communication

Education

High School Diploma or equivalent

Bachelor's degree preferred

Job description

Dm Clinical Research Group in Seattle, WA seeks a Clinical Research Coordinator II to ensure quality studies per sponsor protocol, FDA regulations, and ICH/GCP guidelines.

You will oversee subject visits, data entry, and regulatory documentation, coordinate training, monitor enrollment, and liaise with investigators, lab, and sponsor teams to meet timelines. Strong communication, detail-orientation, multitasking, and 2+ years CRC experience preferred; bilingual English/Spanish preferred.