Certified Medical Assistant (CMA)

Dm Clinical Research Group; Southfield (MI); On-site; USD 42,000 - 58,000; Full time

Job summary

DM Clinical Research Group seeks a Certified Medical Assistant (CMA) to join our clinical team in Southfield, Michigan. The role focuses on dispensing Investigational Products (IP) in accordance with study protocols and sponsor requirements.

Responsibilities include IP management, documentation, audits for accuracy, and collaboration with Investigators and study managers to ensure protocol adherence and patient safety in ongoing trials.

Qualifications

• Associates degree required or 2 years of relevant coursework; Bachelor's degree preferred.
• Licensed or credentialed CMA/LPN preferred as part of qualifications.
• 2+ years of Clinical Research experience, including in-clinic work, required.
• 1+ year of Clinical Research Coordinator experience (Blinded or Unblinded) required.
• 1+ year utilizing CRIO preferred.

Responsibilities

• Study IP management and dispensing of Investigational Products per protocol.

Skills

Communication

Time management

Multitasking

Bilingual Spanish

Computer skills

Education

Associates degree

Bachelor's degree preferred

LPN or CMA credential preferred

Pharmacy Technician Certification preferred

Tools

CRIO

Word

Excel

Outlook

Google Suite

Job description

DM Clinical Research is looking to hire an Certified Medical Assistant (CMA) to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.Duties & Responsibilities:Study IP managementCompound and dispense prescribed IP as needed by Sponsor approved protocolSupervise and maintain records of all medicationsPerform regular audits on the clinical data to assess percent completeness and accuracyProvide consultative support regarding the preparation and dosing of drugsMaintain documentation of IP accountability: receipt, dispensing, return to sponsor/destructionInterpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trialsEnsure 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.KNOWLEDGE & 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 skillsAbility to remain composed under pressure and high-stress situationsOutgoing personalityWell-organized with attention to detail.Must be able to multitask.Bilingual (Spanish) preferred