×
Register Here to Apply for Jobs or Post Jobs. X

Coordinator, Clinical Research Program; Regulatory; Leukemia

Remote / Online - Candidates ideally in
Arlington, Tarrant County, Texas, 76001, USA
Listing for: University of Texas MD Anderson Cancer Center
Remote/Work from Home position
Listed on 2026-10-03
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 27.64 USD Hourly USD 27.64 HOUR
Job Description & How to Apply Below
Position: Coordinator, Clinical Research Program (Regulatory) - Leukemia
Coordinator, Clinical Research Program (Regulatory) - Leukemia

The University of Texas MD Anderson Cancer Center is a world-renowned institution dedicated to cancer patient care, research, education, and prevention. Within the Department of Leukemia, the Coordinator, Clinical Research Program supports complex clinical research operations that advance innovative therapies and improve outcomes for patients with leukemia. The Coordinator, Clinical Research Program plays a critical role in protocol administration, regulatory oversight, and research program coordination.

UT MD Anderson provides an environment where clinical research excellence, collaboration, and continuous improvement are central to its mission. The Coordinator, Clinical Research Program works closely with physicians, study chairs, protocol sponsors, and research staff to ensure clinical trials are developed, activated, managed, and maintained in compliance with institutional and regulatory requirements. The Coordinator, Clinical Research Program also contributes to training, quality assurance, reporting, and grant preparation activities that support departmental research goals.

The ideal candidate will have a bachelor's degree in a scientific, healthcare, business, public health, or related field, along with progressively responsible experience supporting clinical research programs, protocol administration, regulatory compliance, and clinical trial operations. Candidates should demonstrate expertise in coordinating complex research activities, managing protocol submissions and maintenance, ensuring compliance with Institutional Review Board (IRB) and federal regulations, developing reporting and tracking systems, supporting grant preparation efforts, and delivering training programs for research personnel.

Professional certifications related to clinical research administration or coordination are valued, along with strong organizational, project management, analytical, communication, and stakeholder collaboration skills. The successful candidate will be highly detail-oriented, capable of managing multiple priorities in a fast-paced environment, and committed to supporting the research mission of The University of Texas MD Anderson Cancer Center through effective coordination of clinical research programs within the Department of Leukemia.

Minimum $27.64/hour
- Midpoint $34.62/hour
- Maximum $41.59/hour

The typical work schedule is Days

Work Location:

Remote

Why Us?

This role directly supports UT MD Anderson's mission to eliminate cancer through outstanding research and innovation. The position offers opportunities to work with leading faculty and research teams, contribute to impactful clinical trials, develop expertise in regulatory and protocol operations, and maintain work-life balance through a remote work environment.

  • 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
Administrative & Regulatory Operations
  • Provide oversight of clinical research protocol development, administrative processing, and regulatory activities.
  • Collaborate with physicians, study chairs, and protocol sponsors regarding protocol design, planning, implementation, and evaluation.
  • Serve as liaison with research administration offices for…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary