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Certified Medical Assistant (4063)

DM CLINICAL RESEARCH GROUP
Posted 8 days ago, valid for 20 days
Location

Irving, TX, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • DM Clinical Research is seeking a Certified Medical Assistant to work as an Unblinded Clinical Research Coordinator in Dallas, TX.
  • The role involves dispensing Investigational Products, measuring vital signs, collecting specimens, and administering injections.
  • Candidates must have at least 2 years of clinical research experience and 1 year of Clinical Research Coordinator experience.
  • An Associate's Degree is required, with a preference for a Bachelor's degree or secondary/foreign medical graduate status.
  • The position offers a competitive salary, though the specific amount is not disclosed in the job details.

Job DetailsJob 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




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