Certified Medical Assistant (4063)

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

Job Details

Job Location: Dallas, TX - Irving, TX 75061

DM Clinical Research is looking to hire an Certified Medical Assistant to join our team and work as a Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties & Responsibilities

• Compound and dispense prescribed IP as needed by Sponsor approved protocol
• Measure vital signs (blood pressure, pulse, temperature, weight) and document medical histories.
• Collect blood (phlebotomy), urine, and other specimens for testing.
• Administer injections or vaccines, and monitor patients for adverse reactions.
• Provide consultative support regarding the preparation and dosing of drugs
• Run routine tests like EKGs (electrocardiograms).
• Supervise and maintain records of all medications
• Perform regular audits on the clinical data to assess percent completeness and accuracy
• Ensure external sites’ regulatory documents and required site certifications are up to date
• Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
• Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
• Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.

KNOWLEDGE & EXPERIENCE

Education

• Associates Degree required or 2 years of formal educational coursework
• Bachelor's degree, preferred
• Secondary or Foreign Medical Graduate, preferred

Experience

• 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
• 1+ year utilizing CRIO, preferred

Credentials

• LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
• Pharmacy Technician Certification, preferred
• Completion of DMCR-required training, including GCP, OSHA and IATA

Knowledge and Skills

• Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
• Excellent communication and customer service skills, both written and verbal
• Excellent time-management skills
• Bilingual (Spanish) preferred

Qualifications