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Join a world-renowned medical and research center dedicated to excellence and innovation. In this pivotal role, you will coordinate clinical research projects, supervise a dedicated team, and ensure compliance with regulatory standards. Your contributions will directly impact patient care and research outcomes in oncology and hematology trials. With a strong focus on teamwork and professional growth, this position offers a unique opportunity to advance your career in a supportive environment. Be part of a mission-driven organization that values compassion and collaboration.
WHY UT SOUTHWESTERN?
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 number 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!
JOB SUMMARY
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.
ESSENTIAL FUNCTIONS include:
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
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.
BENEFITS
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:
EXPERIENCE AND EDUCATION
Required
JOB DUTIES
SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO Statement
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.