Clinical Research Coordinator II – IP Dispensing & Trials

Paycom - ATS; Southfield (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II to join our team in Detroit/Southfield, MI. The role involves dispensing Investigational Products (IP) per protocol, IP management, and ensuring blinding integrity.

You will train new staff, support startup activities, maintain accurate medication records, and collaborate with the PI, sponsor, and study managers to meet trial requirements. Requires 2+ years in clinical research and CRIO familiarity.

Qualifications

• Associates Degree required or 2 years of formal educational coursework.
• Bachelor's degree preferred.
• Secondary or Foreign Medical Graduate, preferred.
• 2+ years of Clinical Research experience, in-clinic, required.
• 1+ year as Clinical Research Coordinator, Blinded or Unblinded, required.
• 1+ year utilizing CRIO, preferred.

Responsibilities

• Compound and dispense prescribed IP as needed by Sponsor approved protocol.
• Study IP management and inventory control.
• Provide training and guidance for new team members.
• Assist in all aspects of start up activities as required.
• Supervise and maintain records of all medications.
• Ensure compliance with blinding plans and study protocols.
• Perform audits on clinical data for completeness and accuracy.
• Assist in onboarding training for new members.
• Ensure regulatory documents and site certifications are up to date.
• Maintain IP accountability documentation and dosing guidance.

Skills

Communication

Time management

Multitasking

Organized

Bilingual Spanish

Education

Associate degree

Bachelor's degree

Secondary medical graduate

Foreign medical graduate

Tools

CRIO

Microsoft Word

Excel

Outlook

Google Suite

Job description

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II to join our team in Detroit/Southfield, MI. The role involves dispensing Investigational Products (IP) per protocol, IP management, and ensuring blinding integrity.

You will train new staff, support startup activities, maintain accurate medication records, and collaborate with the PI, sponsor, and study managers to meet trial requirements. Requires 2+ years in clinical research and CRIO familiarity.