Cytotechnologist

Full Job Description

This position is located at the Ralph H. Johnson VA Medical Center, Charleston, SC, Pathology & Laboratory Medicine Service.

Applicants pending the completion of educational or certification/licensure requirements may be referred and tentatively selected but may not be hired until all requirements are met.

Basic Requirements: United States Citizenship: Non-citizens may only be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy.

English Language Proficiency: Cytotechnologists must be proficient in spoken and written English. See 38 U.S.C. § 7403(f).

Education: Individuals must have successfully completed a baccalaureate degree from a regionally accredited college/university and successfully completed a Commission on Accreditation of Allied Health Education Programs accredited cytotechnology program.

Foreign Education: To be creditable, education completed outside the U.S.

must have been submitted to a private organization approved by the American Society for Clinical Pathology (ASCP) that specializes in the interpretation of foreign educational credentials and such education must have been deemed at least equivalent to that gained in conventional U.S.

programs. Certification: Candidates must currently possess the Cytotechnologist (CT) (ASCP) or Specialist in Cytotechnology (SCT) (ASCP) certification given by the ASCP Board of Certification.

May qualify based on being covered by the Grandfathering Provision as described in the VA Qualification Standard for this occupation (only applicable to current VHA employees who are in this occupation and meet the criteria).

Grade Determinations: In addition to the basic requirements for employment, the following criteria must be met when determining the grade of candidates: Cytotechnologist GS-11 Experience: The candidate must have one year of creditable experience equivalent to the journey level (GS-9) that is directly related to the position to be filled.

Example of experiences: Independently reviews clinical data of patients and evaluates all cytology preparations by light microscopy for the presence or absence of cellular patterns, presence of micro-organisms, inflammatory reactions, endocrinopathies, benign changes, pre-malignant changes, neoplasia, and cellular responses to therapeutic agents.

The cytotechnologist issues and verifies the final diagnosis for negative gynecologic specimens.

The cytotechnologist prioritizes, prepares, and processes all specimens for cytodiagnostic and immunohistochemical testing in compliance with the guidelines of regulatory agencies.

The cytotechnologist instructs others on the proper collection methods and transportation of specimens and determines acceptability of patient samples for processing.

The cytotechnologist performs routine maintenance of equipment using standard operating procedures. AND NOTE: Advanced assignments may also include one or more of the tasks identified below.

When these duties are required, the Advanced Cytotechnologist must also demonstrate the corresponding advanced KSAs as identified by the corresponding asterisk(s) below in KSA (c) v. - (c) viii.

These KSAs are: **Electron Microscopy (KSA (c) v.): Ability to utilize electron microscope, performance of ultrathin cryomicrotomy, and staining of ultrastructural components.

***Safety Coordination (KSA (c) vi.): Ability to oversee safe handling of specimens, chemicals, and equipment by all staff and ensures adherence to safety regulations.

****Laboratory Education (KSA (c) vii.): Ability to plan and administer an ongoing continuing education program for laboratory staff to meet accreditation requirements.

*****Automated Data Processing Applications Coordinator (KSA (c) viii.): Ability to carry out day-to-day operations related to laboratory information systems/computer use and system maintenance.

(c) Demonstrated Knowledge, Skills, and Abilities. In addition to the experience above, the candidate must demonstrate the KSAs i. - iv.

and the advanced KSA as identified by the corresponding asterisk(s): i.

Ability to independently determine specimen adequacy using complex specialized testing methods or techniques during Endoscopic Ultrasound, Endobronchial Ultrasound, and other Fine Needle Aspiration procedures.

ii.

Knowledge of pre-analytical, analytical, and post-analytical processes to establish and monitor the overall laboratory quality management and quality control program, and initiate corrective action as needed.

iii. Skill in collecting, compiling, and analyzing data for quality assurance, statistics, trends and reports, and implementing quality improvement initiatives. iv.

Skill in researching, testing, validating, and implementing new procedures and equipment. v. **Ability to perform ultrathin microtomy and operate an electron microscope.

Knowledge of microanatomy sufficient to note ultrastructural and microchemical findings.vi.

***Ability to convey knowledge of safety regulations and guidelines such as CAP, JC, and OSHA, and to ensure staff compliance with safety requirements, including continuing education and employee orientation.

vii. ****Knowledge and skill to plan and administer an ongoing continuing education program for the laboratory to meet accreditation standards.

viii.*****Skill to maintain and troubleshoot computers and laboratory system instrumentation.

Reference: For more information on this qualification standard, please visit https://www.va.gov/ohrm/QualificationStandards/. The full performance level of this vacancy is GS-9.

The actual grade at which an applicant will be selected for this vacancy is GS-11 Physical Requirements: See VA Directive and Handbook 5019, Employee Occupational Health Service. Major Duties:

The incumbent performs a broad range of highly complex testing and procedures for the pathological diagnosis of various disease conditions from cellular samples of the human body.

This involves the performance of highly specialized work requiring theoretical knowledge, scientific competence, and unusual professional judgement.

The position requires responsibility for the examination of a wide range of patient samples submitted for evaluation regarding the presence/absence of benign and malignant conditions.

Duties include, but are not limited to the following: Independently performs and monitors processes such as smear preparation, slide fixation, cell block preparation, monolayer filtration processing, and staining.

Responsibilities to troubleshoot and take corrective action.

Performs full range of specialized tasks, including collecting, compiling, and analyzing data according to the laboratory quality management program.

Evaluates the quality and adequacy of all patient samples before accepting and logging them into the section. Prepares and stains cytology slides for all GYN and non-GYN specimens.

Evaluates the quality of all cytology preparations by light microscopy.

Makes diagnoses using a wide range of knowledge of the human body and pathologic processes, including normal/abnormal cellular patterns, inflammatory reactions, presence of microorganisms, benign changes, premalignant conditions, and cellular responses to therapeutic agents.

Work Schedule: Monday - Friday; 08:00am - 4:30pm Telework: Not Available. Virtual: This is not a virtual position.

Functional Statement #: 57398F Relocation/Recruitment Incentives: Not Authorized Permanent Change of Station (PCS): Not Authorized