Clinical Research Coordinator — IP Dispensing & Patient Care

Dm Clinical Research Group; Irving (TX); Presencial; USD 48.000 - 64.000; Jornada completa

Descripción de la vacante

DM Clinical Research is seeking an experienced Certified Medical Assistant to join our team as a Unblinded Clinical Research Coordinator. The role includes dispensing Investigational Products (IP), performing EKGs, recording vitals, and maintaining IP accountability per sponsor protocols.

Responsibilities also cover phlebotomy, specimen collection, injections, adverse reaction monitoring, and ensuring regulatory documents are up to date.

Formación

• Associates Degree required or 2 years of formal educational coursework.
• Bachelor's degree preferred.
• 2+ years of Clinical Research experience, in-clinic preferred.
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required.

Responsabilidades

• Dispense Investigational Products (IP) per protocol.
• Run routine tests like EKGs.
• Maintain IP accountability records.
• Audit clinical data for completeness and accuracy.
• Ensure external site regulatory documents and site certifications are up to date.
• Collect blood, urine, and other specimens for testing.
• Administer injections or vaccines and monitor adverse reactions.
• Provide dosing consults for drugs.

Conocimientos

EKG testing

Vital signs measurement

Communication skills

Time management

Bilingual Spanish

Educación

Associate degree

Bachelor's degree preferred

LPN or CMA preferred

Pharmacy Technician Certification preferred

Herramientas

CRIO system

Microsoft Word

Excel

Outlook

Google Suite

Descripción del empleo

DM Clinical Research is seeking an experienced Certified Medical Assistant to join our team as a Unblinded Clinical Research Coordinator. The role includes dispensing Investigational Products (IP), performing EKGs, recording vitals, and maintaining IP accountability per sponsor protocols.

Responsibilities also cover phlebotomy, specimen collection, injections, adverse reaction monitoring, and ensuring regulatory documents are up to date.