The Lead Clinical Laboratory Scientist performs the full range of laboratory tests and procedures ranging from routine to complex; and provides technical support to the laboratory section staff, entire facility, and clients from other agencies. Acts as a liaison to other sections of the laboratory and the medical center. The location of the position is Pathology and Laboratory Medicine Service, VA North Texas Health Care System (VANTHCS).
BASIC REQUIREMENTS To qualify for appointment to this position, all applicants must possess the following: Citizenship. Be a citizen of the United States (U.S.). Non-citizens may be appointed when it is not possible to recruit qualified citizens in accordance with 38 U.S.C. § 7407(a). Education. A bachelor's degree or higher from an accredited college or university. Certification. (1) Candidates must meet one of the certification options below. (a) Generalist certification as an MLS given by ASCP BOC or AMT. (b) Generalist certification as an MT given by ASCP BOR or AMT. (c) Categorical certification or Specialist certification by ASCP or AMT. NOTE: Categorical and specialist certifications are not acceptable for CLS Generalist positions or lab sections unrelated to the categorical or specialist certification held. Categorical or specialist certifications are acceptable for higher-graded positions within the relevant lab section or one of the non-section specific assignments (including, Ancillary Testing Coordinator, Education Coordinator, Laboratory Information Manager, Quality Manager, Laboratory Manager, Regional Technical Specialist, National Quality and Compliance Agent, Regional Program Manager, Regional Director, Laboratory Director, or National Quality and Compliance Officer). Grade Determinations: Lead Clinical Laboratory Scientist, GS-12. Experience. 1 year of creditable experience equivalent to the next lower grade level is required for all GS-12 assignments. Knowledge, Skills, and Abilities. In addition to the experience or education above, the candidate must demonstrate the following KSAs: (A) Knowledge of medical technology applicable to a wide range of duties to solve complex problems involving diverse aspects of clinical laboratory practice. (B) Skill to maintain, troubleshoot, and repair laboratory instrumentation. (C) Ability to develop procedures for new tests, and modify existing procedures and methods to resolve problems relative to complex and difficult situations. (D) Ability to manage and coordinate daily work activities and assignments in a section. (E) Ability to provide or coordinate staff development and training. (F) Ability to provide guidance and technical direction to a wide variety of individuals including physicians, nurses, and other clinical staff regarding technical aspects of testing, specimen requirements and results. Assignment. For all lead assignments, the individual must spend at least 25% or more of their time performing lead duties over staff one grade level below. The Lead CLS communicates the organization's strategic plan, mission, vision, and values. The Lead CLS identifies, distributes, balances work, coaches, and facilitates with problem solving methods. The Lead CLS prepares reports and maintains records of work status; resolves simple, informal complaints; reports performance, progress, and training needs of the team and on behavioral problems; and provides information on promotions, reassignment, recognition of outstanding performance, and personnel needs. The Lead CLS is responsible for all aspects of operation in their area of specialty, including assignment of work responsibilities, workload management, and completion of assignments for staff at or above the FPL as well as preparation and maintenance of records and reports, analysis of testing methodologies, training, instrumentation, and compliance. The Lead CLS may act as a liaison to the supervisor and other departments/divisions of the medical center for the appropriate laboratory specialty. Duties may include, but are not limited to, orientation and evaluating the competency of assigned staff including identification of continuing education and training needs, coordinating daily activity of the lab section(s), writing or modifying technical procedures, providing technical instruction, ensuring that policies, procedures and regulatory requirements are followed, advising on course of action to follow when results or samples obtained are unacceptable, and coordinating or performing quality control reviews and method verification activities. Preferred Experience: One year credible experience as Clinical Laboratory Scientist at the GS-11 level or higher Demonstrated experience with reviewing quality control and preventative maintenance. Demonstrated experience troubleshooting instrumentation. Demonstrated experience instructing staff and students. Reference: For more information on this qualification standard, please visit https://www.va.gov/ohrm/QualificationStandards/. The actual grade at which an applicant may be selected for this vacancy is in the GS-12 Physical Requirements: Light lifting, under 15 pounds; Light carrying, under 15 pounds; Reaching above shoulder; Use of fingers; Both hands required; Walking (2-4 hours); Standing (2-4 hours); Depth perception; Ability to distinguish basic colors; Ability to distinguish shades of colors; Hearing (aid may be permitted).
Duties include but are not limited to: A Lead, Clinical Laboratory Scientist has specialized training and experience. Employee has advanced knowledge of specialized and complex subject matter extending beyond the duties of test performance. Individual utilizes wide latitude for exercising independent judgement. Incumbent performs the below duties at least 25 percent of the time. - Facilitates team or unit processes by working in collaboration with team members to ensure that tasks, priorities, goals, and achievements are coordinated with management. - Responsible for all aspects of operation in their area of specialty, including assignment of work responsibilities, workload management, and completion of assignments for staff. - Prepares and maintains records and reports, analysis of testing methodologies, training, instrumentation, and compliance. - Acts as a liaison to other departments of the medical center for the appropriate laboratory specialty. - Serves as an expert providing authoritative advice and consultation for more markedly difficult, complex, unique, and/or emerging tests requiring special knowledge. - Advises on course of action to follow when results or samples obtained are unacceptable and coordinating or performing quality control review and method verification activities. - Identifies, defines, and resolves issues associated with complex aspects of data or unique controversial aspects of the testing where no direct precedent exists. - Maintains process control through a multifaceted quality assurance program. - Prepares reports, maintains records, and provides administrative information. Prepares and presents work-related information to the supervisor and upper management. - Performs statistical analysis on quality control, quality assurance monitors, and research data in the appropriate laboratory specialty area. - Modifies or writes technical procedures, providing technical instruction ensuring that policies, procedures, and regulatory requirements are followed. Evaluates the competency of assigned staff including identification or continuing education and training needs. - Is responsible as a primary source of information for maintaining current instrumentation. Is responsible for evaluation of new and evolving developments in laboratory instrumentation and automation. - Ensures compliance with rules and regulations of assorted regulatory agencies such as CAP, T JC, AABB, OSHA, and the National Enforcement Office. Coordinates Quality Control activities with the supervisor. Coordinates proficiency program for the appropriate laboratory section. Work Schedule: Monday - Friday, 7:00am to 4:30pm, Rotating Holidays and Weekends Telework: Not Available Virtual: This is not a virtual position. Functional Statement #: 53488-F EDRP Authorized: Former EDRP participants ineligible to apply for incentive. Contact VISN17EDRP2@va.gov, the EDRP Coordinator for questions/assistance. Learn more Permanent Change of Station (PCS): Not Authorized