Clinical Research Coordinator II: IP Dispensing & Study Ops

Dm Clinical Research Group; Irving (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

DM Clinical Research Group seeks an Unblinded Clinical Research Coordinator II to join our Irving, TX team. You will dispense Investigational Products (IP) and coordinate trial activities in alignment with study protocols.

Ideal candidates have 2+ years in clinical research (1+ year as a coordinator, blinded or unblinded) and IP handling credentials; bilingual Spanish is a plus. This role focuses on IP management, regulatory compliance, and team onboarding.

Qualifications

• 2+ years of Clinical Research experience, inclusive of in-clinic experience.
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, preferred.
• Experience dispensing Investigational Products (IP) and managing IP accountability.
• Familiarity with regulatory documents and site certifications.

Responsibilities

• Compound and dispense prescribed IP per protocol.
• Study IP management and IP accountability records.
• Provide training and guidance for new team members.
• Assist in start-up activities and maintain regulatory documentation.
• Audit clinical data for completeness and accuracy.
• Coordinate with PI, sponsor, and study staff to ensure protocol adherence.

Skills

Communication skills

Time management

Multitasking

Bilingual Spanish

CRIO familiarity

Education

Associate degree or 2 years of coursework

Bachelor's degree preferred

LPN / CMA or Pharmacy Technician Certification preferred

Foreign Medical Graduate (preferred)

Tools

Microsoft Word

Excel

Outlook

Google Suite

Job description

DM Clinical Research Group seeks an Unblinded Clinical Research Coordinator II to join our Irving, TX team. You will dispense Investigational Products (IP) and coordinate trial activities in alignment with study protocols.

Ideal candidates have 2+ years in clinical research (1+ year as a coordinator, blinded or unblinded) and IP handling credentials; bilingual Spanish is a plus. This role focuses on IP management, regulatory compliance, and team onboarding.