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  3. Unblinded Clinical Research Coordinator II (4021)
DM CLINICAL RESEARCH GROUP logo

Unblinded Clinical Research Coordinator II (4021)

DM CLINICAL RESEARCH GROUP·Southfield, Michigan

OtherOn Site2-5 yrsPosted 1 month ago
Practice for this role

Unblinded Clinical Research Coordinator II (4021)

How this role compares

Computed from live listings

  • 28 similar openings in the Southfield area
  • 53 days median time this employer’s postings stay open (last 90 days)

About the role

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.

Job DetailsJob Location

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!

Duties & Responsibilities

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

Requirements

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.

  • associate degree
  • bachelor degree
  • Communication
  • Customer Service
  • Time Management
  • OSHA
  • Microsoft Office
  • Google Suite
  • Data Auditing
  • Clinical Research
  • Regulatory Documentation
  • GCP
  • Protocol Compliance
  • Pharmacy Technician
  • IATA
  • Investigational Product Dispensing
  • CRIO
  • Patient Dosing

Posting details

Employment type
Other
Work arrangement
On Site
Experience
2-5 yrs
Location
Southfield, Michigan
Posted
Jul 30, 2026
Closes
Sep 28, 2026
Application
Employer website
DM CLINICAL RESEARCH GROUP logo

Hiring organization

DM CLINICAL RESEARCH GROUP

DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified...

IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
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Market context

Michigan support-services roles need certified assistants

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.

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