Clinical Research Coordinator II: IP Dispensing & Site Ops

Paycom - ATS; Irving (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

DM Clinical Research in Irving, Texas is seeking an Unblinded Clinical Research Coordinator II to support clinical trials. You will dispense Investigational Products (IP), manage IP accountability, and ensure regulatory documents are current while upholding blinding plans and study protocols.

The role requires 2+ years in clinical research, 1+ year as a coordinator (blinded or unblinded), and relevant certifications or degrees. Strong organization, communication, and data accuracy are essential.

Qualifications

• 2+ years of Clinical Research experience, inclusive of in-clinic experience.
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded.
• LPN or CMA or Pharmacy Technician certification preferred.
• Associates degree required; Bachelor’s degree preferred.

Responsibilities

• Dispense Investigational Products (IP) as per protocol and Sponsor approval.
• Manage IP accountability and storage with temperature reporting.
• Assist in company start-up activities and onboarding of new staff.
• Audit clinical data for completeness and accuracy and ensure regulatory documents are up to date.
• Interpret schedules to plan IP compounding, preparation, and dispensing.
• Provide training and guidance to team members on study procedures and data entry portals.
• Coordinate with PI, Sponsor, study manager, and other coordinators to ensure compliance.

Skills

IP Dispensing

Clinical Research

Documentation

Communication

Education

Associates degree

Bachelor's degree preferred

LPN or CMA preferred

Pharmacy Tech Certification preferred

Tools

CRIO

Microsoft Excel

Google Suite

Microsoft Word

Job description

DM Clinical Research in Irving, Texas is seeking an Unblinded Clinical Research Coordinator II to support clinical trials. You will dispense Investigational Products (IP), manage IP accountability, and ensure regulatory documents are current while upholding blinding plans and study protocols.

The role requires 2+ years in clinical research, 1+ year as a coordinator (blinded or unblinded), and relevant certifications or degrees. Strong organization, communication, and data accuracy are essential.