Supervisor Clinical Research, Simmons Cancer Center

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the No. 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals.

Our highly competitive benefits package offers healthcare, PTO and paid holidays, on‑site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you‿ll discover a culture of teamwork, professionalism, and a rewarding career!

Works under the direction of an Investigator(s) with limited supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Provides supervision to a team engaged in the execution of multiple, complex research protocols.

This position will supervise the Regulatory Assistants/Regulatory Associates (RAs) for oncology and hematology clinical trials.

• Oversees the day-to-day activities of the RA team.
  
  Develop performance standards and expectations for the RA team and periodically assesses the attainment of those standards.
• 2.Manages work schedules and conducts performance reviews for RAs.
• 3.Oversees training for new and existing employees.
• 4.Ensure all training is clearly documented for employee’s file.
• 5.Train new team members during their onboarding.
• 6.Supervision of training for existing team members.
• 7.Organization of regular RA team meetings and oversees creation of agendas as well as meeting minutes.
• 8.Assists Regulatory Operations Manager with activation of studies which includes
• Monitoring activation to identify any additional resources needed or workflows which might need modification.
• Assists in working through any obstacles identified during the submission process
• 8.Maintains working relationships with faculty and academic departments across UTSW to help oversee the conduct of hematology and oncology clinical trials.
• 9.Acts as a working manager role of a RA. Will continue to have studies assigned (while not a full load) while managing the team.
• 10.Work with DOT Managers to prioritize study submissions and manage regulatory monitoring visits and audits.
• 11
  
  Manages the progress of new trials through regulatory submission and approval.
• 12.Recommends and/or creates new policies and procedures for improvement of program compliance activities.
• 13.Quality checks of regulatory binders/essential regulatory documents across the regulatory team.
• 14.Complete and maintain RCR registration process for investigators
• 15. Performs other duties as assigned.

UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

• PPO medical plan, available day one at no cost for full-time employee-only coverage
• 100% coverage for preventive healthcare-no copay
• Paid Time Off, available day one
• Retirement Programs through the Teacher Retirement System of Texas (TRS)
• Paid Parental Leave Benefit
• Wellness programs
• Tuition Reimbursement
• Public Service Loan Forgiveness (PSLF) Qualified Employer
• Learn more about these and other UTSW employee benefits!

Required

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