Lead Clinical Research Supervisor, Radiation Oncology

UT Southwestern Medical Center; Dallas (TX); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

PPO medical plan day one

Paid Time Off day one

Retirement Programs

Paid Parental Leave

Wellness programs

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

Learn more about these and other UT SW

Job summary

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support clinical research projects under investigator supervision. The role focuses on patient/participant coordination, data management, and oversight of multiple complex protocols.

The candidate will supervise a team, monitor HRPP/IRB compliance, assist with study design, budgeting, and regulatory requirements, and ensure timely sponsor reporting.

Qualifications

• Bachelor's Degree in medical or science related field.
• 5 years of clinical research experience.
• Prior experience in the UT Southwestern clinical research mentoring program is highly desirable.
• ACRP or SOCRA certification a plus.

Responsibilities

• Assists with the daily operations for the research unit, to include staffing, protocol management, budgeting, and regulatory requirements.
• May assist in development of study design, implementation, and administration for new studies ensuring compliance with HRPP/IRB requirements, Federal/State regulations, and grant and/or contract parameters.
• Assists with monitoring and oversight of active clinical research protocols in accordance with internal policies, federal and state regulations, and University policies.
• Oversees and coordinates data collection and assures accuracy and timely submission to sponsors and/or external
• Oversees and coordinates the scheduling and efficient usage of research facilities.
• Performs research billing activities (including linking patient calendars) and oversees the financial status of the research protocols for the team
• Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards
• Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing, or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
• Performs other duties as assigned.

Skills

Staffing

Protocol management

Budgeting

Regulatory requirements

Study design

Data collection

Scheduling facilities

Research billing

Patient safety

HRPP/IRB

Education

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support clinical research projects under investigator supervision. The role focuses on patient/participant coordination, data management, and oversight of multiple complex protocols.

The candidate will supervise a team, monitor HRPP/IRB compliance, assist with study design, budgeting, and regulatory requirements, and ensure timely sponsor reporting.