[Hiring] Clinical Laboratory Technologist - Cytogenetics @SIGMA CORE LLC

Role Description

This Job Description is intended to provide a general summary of the duties, responsibilities, qualifications, and expectations associated with the Clinical Laboratory Technologist - Cytogenetics (Remote) position with COREPATH Laboratories / SigmaCore LLC (the "Company"). It is not intended to be an exhaustive list of all duties, responsibilities, qualifications, or working conditions associated with the position. The Company reserves the right to modify, assign, or reassign duties and responsibilities as business needs require.

The Clinical Laboratory Technologist - Cytogenetics (Remote) performs, evaluates, interprets, correlates, and validates laboratory testing procedures and results within the specialty area of cytogenetics. This role analyzes biological specimens using manual and automated methodologies and exercises professional judgment in accordance with established laboratory procedures, regulatory requirements, and applicable professional standards.

This remote position is responsible for performing chromosome analysis and interpretation using Company-approved systems and technologies while maintaining a reliable, wired internet connection and a secure work environment that protects confidential patient information. The incumbent participates in quality assurance activities, supports diagnostic and treatment decisions through accurate laboratory analysis, and provides technical expertise and education to laboratory and healthcare professionals.

Qualifications

• Bachelor's degree from an accredited college or university in biological sciences, chemical sciences, physical sciences, medical laboratory science, or a closely related field.
• American Society for Clinical Pathology Cytogenetics Certification (ASCP-CG) or eligibility to obtain certification within a timeframe approved by the Company.
• Minimum three (3) years of cytogenetics experience, including chromosome analysis.

Requirements

• Performs accurate cytogenetic analysis of metaphase cells using automated imaging systems and other approved methodologies.
• Distinguishes between normal and abnormal cytogenetic findings.
• Reviews and correlates current test results with prior patient findings to identify clinically significant changes.
• Applies knowledge of patient diagnoses, clinical history, and testing indications to support accurate result interpretation.
• Interprets conventional cytogenetic analyses and collaborates with appropriate laboratory personnel on the assignment of ISCN nomenclature.
• Assists in the review and interpretation of conventional cytogenetic and FISH test results.
• Summarizes findings and prepares case reports for review and sign-out by authorized laboratory leadership, pathologists, and/or laboratory directors.
• Generates and enters cytogenetic reports into the Laboratory Information System (LIS) for review and approval.
• Accurately records test results in worksheets, the LIS, and other required laboratory documentation systems.
• Maintains complete, accurate, and timely clinical, technical, and quality documentation.
• Catalogs and files the slides and records in accordance with laboratory record-retention policies and regulatory requirements.
• Communicates test results and relevant technical information clearly, accurately, and promptly to supervisors, pathologists, and laboratory directors.
• Organizes workload, establishes priorities, and manages assigned cases to meet productivity standards, turnaround times, and laboratory deadlines.
• Maintains high levels of quality, accuracy, and efficiency while meeting established performance expectations.
• Assists with specimen processing and other laboratory activities as needed.
• Identifies technical issues and promptly notifies laboratory leadership.
• Performs troubleshooting activities, evaluates corrective actions, and documents findings in accordance with regulatory and laboratory requirements.
• Adheres to quality assurance principles, laboratory best practices, and established safety requirements.
• Complies with all Company policies, laboratory procedures, accreditation standards, and applicable federal, state, and local laws and regulations.
• Maintains the confidentiality, privacy, and security of protected health information (PHI) in accordance with HIPAA and other applicable laws.
• Demonstrates appropriate professional conduct, ethical behavior, communication skills, and interpersonal effectiveness.
• Maintains familiarity with current standard operating procedures (SOPs).
• Assists with the development, implementation, and revision of laboratory procedures as assigned.
• Participates in validation and verification studies for new methodologies, instrumentation, and testing platforms under appropriate supervision.
• Assists with drafting technical documents, competency assessments, and laboratory communications.
• Participates in continuous improvement initiatives designed to enhance quality, efficiency, safety, and operational effectiveness.
• Identifies opportunities for process improvement and communicates recommendations to laboratory leadership.

Benefits

• This position is classified as Non-Exempt under the Fair Labor Standards Act (FLSA) and is eligible for overtime compensation in accordance with applicable federal and state laws.
• Employees in this position are paid for all hours worked and must accurately record all time worked in accordance with Company policies.

Company Description

COREPATH Laboratories / SigmaCore LLC is committed to providing quality laboratory services and ensuring the confidentiality and integrity of patient information.