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DM CLINICAL RESEARCH GROUP·Southfield, Michigan
Unblinded Clinical Research Coordinator II (4021)
Computed from live listings
The Unblinded Clinical Research Coordinator will be responsible for compounding and dispensing investigational products while ensuring strict adherence to study protocols and blinding plans. They will also manage study documentation, perform data audits, and provide training and support to the clinical research team.
Detroit - Southfield, MI 48076DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Pharmacy Technicians, LPN's and CMA's are encouraged to apply!
Compound and dispense prescribed IP as needed by Sponsor approved protocol Study IP management Provide training and guidance for new team members Assist in all aspects of company start up activities as required Supervise and maintain records of all medications Ensure compliance with study-specific blinding plans Perform regular audits on the clinical data to assess percent completeness and accuracy Assist in onboarding training for new members Ensure external sites’ regulatory documents and required site certifications are up to date Provide consultative support regarding the preparation and dosing of drugs Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials Understand and apply all applicable site procedures Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting Develop operating procedures, guides and best practices for data entry portals and project workflows Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood. Any other duties or tasks assigned by the manager 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 Ability to remain composed under pressure and high-stress situations Outgoing personality Well-organized with attention to detail. Must be able to multitask. Bilingual (Spanish) preferred Qualifications
Candidates must have at least 2 years of clinical research experience, including in-clinic experience, and an associate degree or equivalent coursework. Preferred qualifications include a background as a Pharmacy Technician, LPN, or CMA, along with proficiency in clinical research software like CRIO.
Market context
In Michigan, support-services roles in healthcare often stay active because clinics and practices need dependable staff who can handle patient-facing and back-office tasks. These positions are competitive because employers commonly require a high school diploma, completion of a competency-based medical assistant training program, and timely BLS plus a recognized Medical Assistant certification. Review the AI-summarized requirements and benefits here to quickly compare fit and confirm your certification timeline before applying.