IP-Dispensing Clinical Research Coordinator II

Dm Clinical Research Group; Sugar Land (TX); On-site; USD 60,000 - 85,000; Full time

Job summary

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II in Sugar Land, TX to dispense Investigational Products and manage study IPs. You will train new staff and assist startup activities while ensuring compliance with blinding plans and regulatory standards.

The role requires 2+ years in clinical research and 1+ year as a coordinator, with CRIO experience preferred. Bilingual Spanish is a plus in a diverse team environment.

Qualifications

• 2+ years of Clinical Research experience, in-clinic experience included.
• 1+ year as Clinical Research Coordinator, Blinded or Unblinded, required.
• LPN/CMA or Pharmacy tech background preferred.

Responsibilities

• Compound and dispense Investigational Products per protocol.
• Study IP management and accountability records.
• Provide training and guidance for new team members.
• Support startup activities and regulatory readiness.
• Supervise medication records and storage.
• Ensure adherence to blinding plans and audits of data.

Skills

IP Dispensing

Study Coordination

Regulatory Compliance

Medical Terminology

Spanish language

Education

Associates Degree

Bachelor's degree

Foreign Medical Graduate

Tools

CRIO

Job description

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II in Sugar Land, TX to dispense Investigational Products and manage study IPs. You will train new staff and assist startup activities while ensuring compliance with blinding plans and regulatory standards.

The role requires 2+ years in clinical research and 1+ year as a coordinator, with CRIO experience preferred. Bilingual Spanish is a plus in a diverse team environment.