Certified Pharmacy Technician

Dm Clinical Research Group; Irving (TX); On-site; USD 48,000 - 64,000; Full time

Job summary

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.

Qualifications

• 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.

Responsibilities

• 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.

Skills

EKG testing

Vital signs measurement

Communication skills

Time management

Bilingual Spanish

Education

Associate degree

Bachelor's degree preferred

LPN or CMA preferred

Pharmacy Technician Certification preferred

Tools

CRIO system

Microsoft Word

Excel

Outlook

Google Suite

Job description

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:Run routine tests like EKGs (electrocardiograms).Supervise and maintain records of all medicationsPerform regular audits on the clinical data to assess percent completeness and accuracyEnsure external sites’ regulatory documents and required site certifications are up to dateMaintain documentation of IP accountability: receipt, dispensing, return to sponsor/destructionEnsure receipt and proper storage of IP and bioretention samples, including temperature reportingInteract with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.Compound and dispense prescribed IP as needed by Sponsor approved protocolMeasure 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 drugsKNOWLEDGE & EXPERIENCEEducation:Associates Degree required or 2 years of formal educational courseworkBachelor's degree, preferredSecondary or Foreign Medical Graduate, preferredExperience:2+ years of Clinical Research experience, inclusive of in-clinic experience, required1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required1+ year utilizing CRIO, preferredCredentials:LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferredPharmacy Technician Certification, preferredCompletion of DMCR-required training, including GCP, OSHA and IATAKnowledge and Skills:Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.Excellent communication and customer service skills, both written and verbalExcellent time-management skillsBilingual (Spanish) preferred