Senior CRC: Site Ops & Data Quality

Dm Clinical Research Group; Seattle (WA); On-site; USD 65,000 - 90,000; Full time

Job summary

Dm Clinical Research Group seeks a Clinical Research Coordinator II to ensure high-quality research at assigned investigative sites in line with sponsor protocols, FDA regulations, and ICH-GCP guidelines. The role aims to meet enrollment expectations and timely project goals.

The CRC II will lead study visits, ensure data integrity, follow ALCOA-C standards, and communicate with investigators, sponsors, and project teams to support safe and compliant trial conduct.

Qualifications

• Proficient communication and comprehension in English (verbal and written).
• Bi-lingual English/Spanish communication preferred.

Responsibilities

• Complete required training (ICH-GCP, IATA, protocol-specific) before study start.
• Conduct study visits and protocol-required procedures with timely documentation.
• Maintain ALCOA-C compliant documentation and data entry with timely query resolution.
• Coordinate with Laboratory, Data, Administrative, Investigators, and Sponsor/CRO teams.
• Ensure adherence to FDA regulations, ICH-GCP guidelines, and study protocols at sites.
• Monitor enrollment goals and communicate progress to management.

Skills

Communication skills

Bilingual English/Spanish

Detail oriented

Education

Bachelor's degree preferred

High School Diploma or equivalent

Foreign Medical Graduates preferred

Job description

Dm Clinical Research Group seeks a Clinical Research Coordinator II to ensure high-quality research at assigned investigative sites in line with sponsor protocols, FDA regulations, and ICH-GCP guidelines. The role aims to meet enrollment expectations and timely project goals.

The CRC II will lead study visits, ensure data integrity, follow ALCOA-C standards, and communicate with investigators, sponsors, and project teams to support safe and compliant trial conduct.