Job Description

The *Hematology Laboratory at MD Anderson* plays a vital role in delivering timely, accurate, and high-complexity diagnostic testing that directly supports cancer diagnosis, treatment decisions, and clinical outcomes. As one of the institution's busiest and most advanced laboratories, Hematology provides comprehensive testing services that help clinicians monitor disease progression, evaluate therapy effectiveness, and deliver exceptional patient care. Our team operates in a highly collaborative, fast-paced environment where precision, innovation, and continuous improvement are essential. As a *Clinical Laboratory Supervisor in Hematology*, you will provide both technical and operational leadership to ensure high-quality testing and seamless laboratory operations. This role is ideal for an experienced MLS professional with strong leadership, troubleshooting, and regulatory knowledge who is ready to guide a team, oversee complex workflows, and lead initiatives in quality, process improvement, and validation of new technologies. You will play a key role in staff development, competency assessment, SOP management, regulatory readiness, and strategic planning-all of which contribute to a culture of excellence within the Hematology Laboratory. MD Anderson is proud to offer a *comprehensive benefits package*, including *paid medical benefits, PTO, retirement plans, and more*, giving you the support and stability you need to grow your leadership career while maintaining a strong work-life balance. **The ideal candidate will have Hematology experience along with 2 years of supervisor/managerial experience** **JOB SPECIFIC COMPETENCIES** **Technical Leadership ** - Supervises the daily activities in a clinical laboratory. - Is a subject matter expert in assigned laboratory section - Supervises employees and assists with trouble shooting efforts of challenging processes or procedures - Leads troubleshooting of computer functions and ensures all employees are competent and able to perform computer functions. - Oversee coordination and ensure maintenance of policies and procedures for all clinical testing. - Reviews and updates SOPs in a timely manner to ensure that current practices are in alignment with approved procedures. - Leads the evaluation and validation of new methodologies, tests, and instrumentation. - Assists with LIS applications implementation, testing and recommends modifications as needed. - Perform clinical lab assays, tests, and procedures as necessary to ensure optimal patient care services. **Productivity, Supervision, and Teambuilding** - Ensures all employees are trained and guides new employee development. - Ensures productivity standards are met by team members as well as coaches and counsels to improve performance when needed. - Discovers, develops and leads process improvements that positively impact productivity and laboratory function. - Ensures all testing phases (including pre-analytical, analytical, and post-analytical) of laboratory testing are performed in alignment with laboratory policies and procedures. - Provides a team environment that promotes cohesiveness, communication, respect, helpfulness, and desire for excellence. - Demonstrates availability, approachability, and the desire to help, encourage and respond to others. - Manages personnel activities such as performance evaluations, disciplinary actions, staff scheduling, staff coaching and mentoring, among others, in compliance with the institutional, divisional, and departmental policies and procedures. - Ensures supplies and equipment are ordered and maintained to meet laboratory testing needs. **Quality Oversight** - Ensures the staff compliance with all regulatory and accreditation requirements and safety standards. - Performs or oversees competency assessment of all testing personnel in compliance with the regulatory requirements. - Participates in the strategic development of employees and of process improvements that positively impact the productivity, function and future direction of the laboratory. - Oversees the new procedures, lab bulletin, test cost analysis, business plan, competency tests and training of other employees for the new tests, processes or instrumentation. - Ensures adequate quality control, quality assurance and quality improvement methods are implemented and performed. -Reviews and updates SOPs in a timely manner to meet CAP regulations. - Participates in quality assurance program - Oversees the Proficiency testing program according to CAP regulations. Other duties as assigned Required Education: Bachelor's degree in a related science field or Molecular Genetic Technology or successful completion of a National Accrediting Agency for Clinical Laboratory Science (NAACLS) accredited Clinical Laboratory Science/Molecular Genetic Technology accredited program. Preferred: Master's Degree or Doctorate in a related science field. Required Experience: Eight years of experience in a clinical laboratory compliance and operations to include three years of lead or supervisory experience. Six years experience in clinical laboratory compliance and operations to include three years of lead or supervisory experience with Master's degree. Four years of experience in a clinical laboratory compliance and operations to include three years of lead or supervisory experience with Doctorate degree. Two years of laboratory experience required may be substituted for required certification. Must pass pre-employment skills test as required and administered by Human Resources. 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. Required Certification: One of the following: Technologist/Scientist certification or international in Blood Banking (BB), Chemistry (C), Cytogenetics (CG), Histology (HT), Hematology (H), Histotechnologist (HTL), Microbiology (M), Medical Laboratory Scientist (MLS) or Molecular Biology (MB) by the American Society of Clinical Pathologists (ASCP) Board of Registry (BOR) OR Certified Histocompatability Technologist by the American Society of Histocompatability and Immunogenetics (ASHI) OR Medical Technologist (MT) or Molecular Diagnostics Technologist (MDT) by the American Medical Technologists (AMT). It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. Additional Information * Requisition ID: 177744 * Employment Status: Full-Time * Employee Status: Regular * Work Week: Days * Minimum Salary: US Dollar (USD) 101,000 * Midpoint Salary: US Dollar (USD) 126,500 * Maximum Salary : US Dollar (USD) 152,000 * FLSA: exempt and not eligible for overtime pay * Fund Type: Hard * Work Location: Onsite * Pivotal Position: Yes * Referral Bonus Available?: Yes * Relocation Assistance Available?: Yes \#LI-Onsite

Job Tags

Full time, Local area, Relocation package,

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