LabCorp offers opportunities with advancement potential in an influential and expanding company.  Be a part of something where you can make an impact on improving health and improving lives. 

Schedule: Tuesday - Saturday (10am - 6:30p)

Benefits: All job offers will be based on a candidate?s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable.  For more detailed information, please click here.

Job Responsibilities:

• Assist with data for monthly reports
• Review the daily workload of ?negative? cases for a minimum of 10% quality control review
• Generate a final report regarding the unsatisfactory cases on a daily basis
• Provide a render of final diagnosis for cases designated for triage
• Review follow-up clinical information and biopsy correlation when available
• Screen and evaluate any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions
• Screening of all liquid based cytology, both manual and imaged, as well as conventional slides
• Perform microscopic evaluation of cytological specimens following laboratory procedures and workload policies
• Ensure proper documentation of workload recording, including screening and non-screening activities as required by CLIA and laboratory guidelines
• Maintain absolute integrity in the accurate performance and reporting of results
• Meet slide screening requirements as per standard operating procedure
• Finalize testing results into the computer in an accurate and timely manner
• Provide backup for cytology processing and other tasks as needed
• Comply with all safety, infection control and HIPAA policies

 Requirements:

• Bachelor of Science degree from an accredited college/university
• Successful completion of an accredited Cytology program
• ASCP Cytotechnologist (CT) Certification is required
• 1 year of experience as a Cytotechnologist
• ThinPrep and SurePath certifications is a plus
• Must pass slide screening requirements and annual CAP proficiency test
• Demonstrated understanding of Cyto preparation techniques
• Automated and non-automated testing experience is preferred
• Familiarity with laboratory information systems (LIS)
• Ability to work independently or within a team
• Highly organized and strong attention to detail
• Strong communication skills; both written and verbal
• Must be able to pass a standardized color vision screen

If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!