Clinical Research CMA & Coordinator (Unblinded Trials)

Dm Clinical Research Group; Irving, Dallas (TX, TX); On-site; USD 52,000 - 76,000; Full time

Job summary

DM Clinical Research is seeking a Certified Medical Assistant to join as an Unblinded Clinical Research Coordinator. The role involves dispensing investigational products and coordinating with investigators to ensure protocol compliance.

Responsibilities include vital signs, specimen collection, injections, EKGs, IP accountability, data audits, and maintaining site regulatory documents. Clinical research experience and GCP/OSHA/IATA training are preferred.

Qualifications

• Associates degree or 2 years of formal coursework are required.
• Bachelor's degree is preferred.
• Secondary or foreign medical graduate is preferred.

Responsibilities

• Compound and dispense Investigational Products per sponsor protocol.
• Measure vital signs and document medical histories.
• Collect blood, urine, and other specimens for testing.
• Administer injections or vaccines; monitor adverse reactions.
• Provide consultative support on drug preparation and dosing.
• Run routine tests like EKGs and supervise medications.
• Audit clinical data for completeness and accuracy.
• Ensure site regulatory documents and certifications are up to date.
• Maintain IP accountability: receipt, dispensing, and return/destruction.
• Ensure proper storage of IP and samples with temperature reporting.
• Coordinate with PI, sponsor, study manager and other coordinators.

Skills

Computer proficiency

Communication skills

Time-management

Bilingual (Spanish) preferred

Education

Associate degree or 2 years coursework

Bachelor's degree preferred

Secondary or Foreign Medical Graduate, preferred

Tools

CRIO

Job description

DM Clinical Research is seeking a Certified Medical Assistant to join as an Unblinded Clinical Research Coordinator. The role involves dispensing investigational products and coordinating with investigators to ensure protocol compliance.

Responsibilities include vital signs, specimen collection, injections, EKGs, IP accountability, data audits, and maintaining site regulatory documents. Clinical research experience and GCP/OSHA/IATA training are preferred.