Manager - Clinical Protocol Admin / Nuclear Medicine
Full-time
MD Anderson
The University of Texas MD Anderson Cancer Center is dedicated to eliminating cancer in Texas, the nation, and the world through integrated programs in patient care, research, prevention, and education. Within the Nuclear Medicine Department, the Manager of Clinical Protocol Administration provides operational leadership for clinical research programs supporting theranostics and radiopharmaceutical research initiatives within Diagnostic Imaging. The Manager of Clinical Protocol Administration in the Nuclear Medicine dept oversees clinical research operations, multidisciplinary coordination, regulatory compliance, and strategic program development. The Manager of Clinical Protocol Administration plays a central role in trial activation, research program execution, and stakeholder collaboration, while supporting the continued growth of the research portfolio at UT MD Anderson. a { text-decoration: none; color: #464feb; } tr th, tr td { border: 1px solid #e6e6e6; } tr th { background-color: #f5f5f5; } The ideal candidate will possess a Master's degree or higher (preferred, not required) in Science, Healthcare, Nursing, or a related field, combined with substantial experience in program and project management. Candidates with a background in clinical research, particularly within oncology, nuclear medicine, theranostics, molecular imaging, or related clinical settings, are highly preferred. The successful candidate will be a proactive, highly organized, and collaborative clinical research professional with a demonstrated ability to manage complex research programs and initiatives. They will possess strong expertise in research operations, protocol management, regulatory compliance, stakeholder engagement, and cross-functional coordination. This individual will excel at building and maintaining productive relationships with internal and external stakeholders, addressing operational challenges, optimizing workflows, and fostering multidisciplinary collaboration. Additionally, the candidate should have a proven track record of supporting and advancing clinical research programs, with the ability to drive strategic initiatives that contribute to the continued growth and success of MD Anderson's Theranostics and Molecular Imaging Research Program. Why Us? At UT MD Anderson, this role directly supports the advancement of innovative theranostics and radiopharmaceutical research programs that contribute to improved cancer diagnosis and treatment. The position offers the opportunity to lead complex clinical research initiatives, collaborate with multidisciplinary experts, influence program growth, and contribute to a mission-driven organization committed to patient care, research, education, and prevention while supporting professional development and work-life balance. • Employer-paid medical coverage starting day one for employees working 30+ hours/week, plus optional group dental, vision, life, AD&D, and disability insurance.
• Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options.
• Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.
• Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Clinical Research Operations & Trial Activation • Lead operational feasibility reviews for radiopharmaceutical and theranostics research protocols
• Direct trial activation planning and study readiness activities
• Coordinate study startup requirements across participating teams
• Manage resource planning and operational workflow development
• Resolve operational issues affecting study activation and execution
• Monitor protocol progress, activation milestones, and action items throughout study lifecycles Multidisciplinary Coordination & Care Pathway Management • Serve as the central liaison among Nuclear Medicine, disease-specific clinical teams, research staff, Radiation Safety, Imaging Physics, and external stakeholders
• Coordinate patient care pathway components within research protocols
• Align evaluations, imaging, laboratory testing, treatment planning, scheduling, and follow-up activities across teams
• Facilitate communication and operational coordination supporting patient progression through theranostics clinical trials Research Program Oversight & Regulatory Compliance • Oversee study activities to ensure compliance with protocol requirements
• Ensure adherence to institutional policies, IRB requirements, radiation safety regulations, and applicable federal guidelines
• Support research governance, patient safety, and quality oversight initiatives
• Promote operational excellence across the theranostics research portfolio
• Partner with investigators and leadership to support clinical research objectives
• Address operational barriers affecting study execution as needed Strategic Program Development & Growth • Support expansion of radiopharmaceutical imaging and theranostics research programs
• Assist with strategic planning and long-term program growth initiatives
• Optimize operational workflows and research infrastructure
• Contribute to staffing initiatives and stakeholder partnership development
• Foster collaboration with internal departments, national organizations, and industry sponsors
• Advance research initiatives and program objectives through strategic engagement Perform other duties as assigned EDUCATION
• Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options.
• Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.
• Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Clinical Research Operations & Trial Activation • Lead operational feasibility reviews for radiopharmaceutical and theranostics research protocols
• Direct trial activation planning and study readiness activities
• Coordinate study startup requirements across participating teams
• Manage resource planning and operational workflow development
• Resolve operational issues affecting study activation and execution
• Monitor protocol progress, activation milestones, and action items throughout study lifecycles Multidisciplinary Coordination & Care Pathway Management • Serve as the central liaison among Nuclear Medicine, disease-specific clinical teams, research staff, Radiation Safety, Imaging Physics, and external stakeholders
• Coordinate patient care pathway components within research protocols
• Align evaluations, imaging, laboratory testing, treatment planning, scheduling, and follow-up activities across teams
• Facilitate communication and operational coordination supporting patient progression through theranostics clinical trials Research Program Oversight & Regulatory Compliance • Oversee study activities to ensure compliance with protocol requirements
• Ensure adherence to institutional policies, IRB requirements, radiation safety regulations, and applicable federal guidelines
• Support research governance, patient safety, and quality oversight initiatives
• Promote operational excellence across the theranostics research portfolio
• Partner with investigators and leadership to support clinical research objectives
• Address operational barriers affecting study execution as needed Strategic Program Development & Growth • Support expansion of radiopharmaceutical imaging and theranostics research programs
• Assist with strategic planning and long-term program growth initiatives
• Optimize operational workflows and research infrastructure
• Contribute to staffing initiatives and stakeholder partnership development
• Foster collaboration with internal departments, national organizations, and industry sponsors
• Advance research initiatives and program objectives through strategic engagement Perform other duties as assigned EDUCATION
- Required: Bachelor's Degree Science, Healthcare, Nursing or related field.
- Preferred: Master's Degree Science, Healthcare, Nursing or related field.
- Required: 6 years Extensive research administrative experience in a biotechnology or academic setting to include two years experience with research protocols, grants and contracts. and
- Required: 2 years Supervisory/management experience.
- May substitute additional experience for required education (or vice versa) on a one to one year basis.
- Successful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience. Completion of both programs can be substituted for a maximum of two years of supervisory or management experience.
- Requisition ID: 183912
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Days
- Minimum Salary: US Dollar (USD) 95,000
- Midpoint Salary: US Dollar (USD) 118,500
- Maximum Salary : US Dollar (USD) 142,000
- FLSA: exempt and not eligible for overtime pay
- Fund Type: Hard
- Work Location: Hybrid Onsite/Remote
- Pivotal Position: Yes
- Referral Bonus Available?: No
- Relocation Assistance Available?: Yes
Vacancy posted 1 day ago
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