Certified Medical Assistant - Clinical Research Coordinator

Dm Clinical Research Group; Seattle (WA); On-site; USD 60,000 - 80,000; Full time

Job summary

DM Clinical Research Group in Seattle, WA seeks a Medical Assistant - Certified (MA-C) to join as an Unblinded Clinical Research Coordinator.

You will dispense Investigational Products (IP), measure vital signs, collect blood and urine samples, administer injections, and run routine tests such as EKGs while ensuring IP accountability and regulatory documentation. Ideal candidates have 2+ years in clinical research, CRIO experience, and bilingual Spanish is a plus.

Qualifications

• Associates degree or 2 years of formal coursework.
• 2+ years of Clinical Research experience, in-clinic.
• 1+ year as Clinical Research Coordinator, Blinded or Unblinded.
• 1+ year using CRIO system.
• LPN or MA-C credential preferred.
• DMCR required training including GCP, OSHA and IATA.

Responsibilities

• Compound and dispense IP as per Sponsor protocol.
• Measure vital signs and document medical histories.
• Collect blood, urine and specimens for testing.
• Administer injections or vaccines and monitor adverse reactions.
• Provide consultative support on drug preparation and dosing.
• Run routine tests like EKGs and maintain IP records.
• Ensure site regulatory documents and certifications are up to date.
• Maintain IP accountability: receipt, dispensing, return or destruction.
• Coordinate with PI, sponsor and study team to meet protocol requirements.

Skills

Computer skills

Communication skills

Time management

Bilingual (Spanish)

Education

Associates Degree

Bachelor’s degree

Foreign Medical Graduate

Tools

CRIO

Job description

DM Clinical Research Group in Seattle, WA seeks a Medical Assistant - Certified (MA-C) to join as an Unblinded Clinical Research Coordinator.

You will dispense Investigational Products (IP), measure vital signs, collect blood and urine samples, administer injections, and run routine tests such as EKGs while ensuring IP accountability and regulatory documentation. Ideal candidates have 2+ years in clinical research, CRIO experience, and bilingual Spanish is a plus.