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Asset & Wealth Management, PWM, Center of Excellence – NPWA Client Implementation, Wealth Management Professional - Analyst
Dallas, Texas, United States · On-site
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Full-time
bachelor degree, postgraduate degree
PPO medical plan, Preventive healthcare coverage, Paid Time Off, Retirement Programs through the Teacher Retirement System of Texas (TRS), Paid Parental Leave Benefit, Wellness programs
Posted 12d ago
~40 hrs/week
Responsibilities
Lead and manage complex clinical research projects for the Sickle Cell program, overseeing timelines, regulatory compliance, and IRB submissions. Coordinate study visits, manage research contracts, and support grant applications and scholarly publications.
Requirements
Requires a Bachelor's degree in a related field and 5 years of clinical research experience, including at least 3 years in project management. An advanced degree and experience with the UTSW clinical research mentoring program are preferred.
Full job description
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 Work under moderate supervision to initiate and manage research projects and programs within a department.
This position will be overseeing the planning, implementation, and management of research projects for Dr. Martin's Sickle Cell program, ensuring alignment with defined scientific objectives and allocated effort, working directly with study Principal Investigators (Pl).
Project Leadership: Lead and manage complex research projects and study timelines.
Contracts & Agreements Management: Oversee research contracts, subawards, and sponsor agreements.
Study Start-Up & Regulatory Oversight: Manage IRB submissions, regulatory compliance, and multisite studies.
Project Coordination & Process Development: Develop workflows, improve processes, and coordinate stakeholders.
Data Management & Chart Abstraction: Maintain databases, ensure data quality, and support reporting and analysis.
Study Visit Coordination & Conduct: Coordinate research visits and ensure protocol compliance.
Participant Tracking & Retention: Support participant recruitment, enrollment, and long-term follow-up.
Communication: Collaborate with investigators, sponsors, regulatory offices, and external partners.
Grantsmanship & Scholarly Products: Support grant applications, manuscripts, abstracts, and presentations.
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:
PPO medical plan, available day one at no cost for full-time employee-only coverage
100%25 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
Experience 5 years experience in clinical research, including at least three years‿ experience in project management, which may include management of specific clinical trials or clinical trials-related programs.
Preferred
Education Advanced degree preferred.
Experience Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional experience.
JOB DUTIES
For new research projects or programs, define project/program scope with the PI, goals and deliverables that support business goals in collaboration with the Clinical Research Manager, Clinical Department Administrator, and Vice Chair/Chair; assist PI to develop project plans, timelines, and associated communications documents; clearly and timely communicate project expectations to team members and management.
Estimate research resources and personnel needed to achieve project/program goals, and work with CRM to help allocate from within the department or externally.
Set and continually manage research project expectations with PIs and other team members; delegate tasks and responsibilities to appropriate personnel; identify and resolve issues and conflicts within the research team or program; identify and manage related issues.
Plan and schedule project timelines and milestones using appropriate tools; track project milestones and deliverables; develop and deliver progress reports.
Compose, edit, or create research personnel training documents. Align business processes with systems changes and provide a mechanism to deliver information to staff and/or faculty as necessary.
Develop best practices and tools for research project execution and management.
Work with PIs on scientific writing in grant proposal development, IRB development.
Coordinate execution of clinical trials following trial guidelines.
May supervise staff in performance of duties.
Performs other duties as assigned.
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 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.