Clinical Research Coordinator II: IP Dispensing & Study Ops

Paycom - ATS; Dallas, Irving (TX, TX); On-site; USD 55,000 - 75,000; Full time

Job summary

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II in Dallas/Irving, TX area to handle dispensing of Investigational Products (IP) and study IP management. You will ensure IP accountability, support regulation readiness, and assist with site training while collaborating with investigators and sponsors.

The role requires 2+ years in clinical research, 1+ year as a coordinator (blinded or unblinded), and potential CRIO experience.

Qualifications

• Associates degree or 2 years of relevant coursework required.
• Bachelor's degree preferred.
• DMCR-required training incl. GCP, OSHA and IATA.

Responsibilities

• Dispense Investigational Products (IP) per sponsor protocol and maintain accurate IP records.
• Manage study IP and ensure compliance with blinding plans.
• Provide training and guidance for new team members.
• Support startup activities and onboarding of new staff.
• Supervise medication records and ensure proper storage and accountability of IP.

Skills

Communication

Time management

Multitasking

Attention to detail

Bilingual (Spanish)

Computer skills

MS Office

Education

Associate degree

Bachelor degree preferred

Foreign medical graduate preferred

Tools

CRIO

Job description

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II in Dallas/Irving, TX area to handle dispensing of Investigational Products (IP) and study IP management. You will ensure IP accountability, support regulation readiness, and assist with site training while collaborating with investigators and sponsors.

The role requires 2+ years in clinical research, 1+ year as a coordinator (blinded or unblinded), and potential CRIO experience.