Lead Clinical Research Supervisor, Radiation Oncology

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical plan (PPO)

Paid Time Off

Retirement programs

Parental leave

Wellness programs

Tuition reimbursement

PSLF eligible employer

Comprehensive benefits package

Job summary

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support Investigator-led studies, coordinating patient/participant activities and data management across multiple protocols.

You will supervise a team, ensure HRPP/IRB compliance, budgeting, and regulatory requirements, and help design and oversee study execution. Strong clinical research experience and a Bachelor's degree in a medical or science field are required; CPR/ACRP or SOCRA certification is a plus.

Qualifications

• Bachelor's Degree in medical or science related field.
• 5 years of clinical research experience.
• May count advanced degree or additional experience in lieu of education or experience.

Responsibilities

• Assists with daily operations for the research unit, including staffing, protocol management, budgeting and regulatory requirements.
• Assist in development of study design, implementation, and administration for new studies with HRPP/IRB compliance.
• Monitor and oversee active clinical research protocols per policies and regulations.
• Oversee data collection and timely submission to sponsors.
• Coordinate scheduling and efficient use of research facilities.
• Perform research billing activities and oversee financial status of protocols.
• Monitor patient safety and ensure reporting per protocol and HRPP standards.
• Duties may involve direct patient interaction and handling of human-subjects records.

Skills

Clinical coordination

Team supervision

Budgeting support

Education

Bachelor's Degree in medical or science related field

5 years of clinical research experience

Job description

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support Investigator-led studies, coordinating patient/participant activities and data management across multiple protocols.

You will supervise a team, ensure HRPP/IRB compliance, budgeting, and regulatory requirements, and help design and oversee study execution. Strong clinical research experience and a Bachelor's degree in a medical or science field are required; CPR/ACRP or SOCRA certification is a plus.