Senior Clinical Research Supervisor & Protocol Lead

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Healthcare benefits

PTO and paid holidays

On-site childcare

Merit increases

Job summary

UT Southwestern Medical Center is seeking a Clinical Research Coordinator to coordinate multiple research projects under limited supervision in Dallas, TX. The role focuses on patient/participant coordination and may involve data management for smaller departments.

You will write SOPs, create training materials, conduct internal audits, assist with study protocols, and manage IRB communications while supervising two junior staff along with regulatory oversight.

Qualifications

• Bachelor's Degree in medical or science related field.
• 5 years of clinical research experience. May consider additional years or advanced degree in lieu of education or experience.
• Prior experience in mentoring or mentoring programs highly desirable.

Responsibilities

• Write and update standard operating procedures for the clinical research team.
• Create training material for new clinical research staff.
• Perform internal regulatory audits of all currently open clinical trials.
• Assist in development and writing of new study protocols.
• Oversee submissions and communications with external central IRBs.
• Coordinate regulatory compliance with CROs and sponsors and lead audit responses.
• Supervise two lower level clinical research staff.

Skills

Clinical research terminology

Computer skills (spreadsheets, Databs)

Effective communication

PHI regulations

Problem solving

Confidential data handling

Education

Bachelor's Degree in medical or science related field

Tools

Interactive web-based software

Job description

UT Southwestern Medical Center is seeking a Clinical Research Coordinator to coordinate multiple research projects under limited supervision in Dallas, TX. The role focuses on patient/participant coordination and may involve data management for smaller departments.

You will write SOPs, create training materials, conduct internal audits, assist with study protocols, and manage IRB communications while supervising two junior staff along with regulatory oversight.