Cytology Technical Specialist

Full time, Monday-Friday, 7:00am-3:30pm

• →Performs all the duties of a Cytotechnologist, to include but not limited to: evaluates patient samples to determine presence or absence of malignant and pre-malignant, infectious and inflammatory processes. Demonstrates expertise in working and theoretical knowledge of diagnostic principles and interpretation of gynecologic and non-gynecologic evaluations. Follows workload policies required by Clinical laboratories Improvement Amendment of 1988 (CLIA '88).
• →Functions as technical expert in Cytological evaluations and processes, performs high complexity testing and is resource on the most complex technical analyses and interpretations. Provides technical expertise and assists Cytotechnologists, data entry and prep staff. Provides technical expertise to any site as needed; provides technical consultation to both internal and external clients.
• →May report, sign-out and troubleshoot cytology responsibilities of molecular testing.
• →Maintains current knowledge of all technical aspects of Cytology and computer functions. Follows technical Quality Control (QC) review policy. Acts as a technical QC tech reviewing slides for qualifying cases. Implements and monitors the regulatory/accrediting and compliance standards of the cytology department. Coordinates orientation and training of new caregivers. Monitors staff development and trains as needed.
• →May assist the Supervisor with following scheduling staff, payroll activities, Inventory control, quality assurance activities and Inter/intra departmental problem solving. Works with the supervisor to develop and implement testing protocols, quality control and quality assurance/policies; may be responsible for the validation processes. Assists in writing new technical procedures/policies and revising current procedures/policies.
• →Investigates and resolves technical problems related to patient/specimen identification, problem requisitions and problems related to cytology cases including cases for rejection.
• →Monitors the preventative maintenance programs for completion and problems. Monitors daily and monthly department Quality Assurance (QA) reports, and identifies potential issues and solutions.
• →Shares candid observations regarding attendance, performance, and staff issues with the Supervisor. Supports the Supervisor in a consistent and objective manner.
• →Supports change efforts within the organization and contributes to their successful implementation. Maintains current knowledge of and complies with of all pertinent policy and procedure manuals. Documents all appropriate information for quality assurance/improvement according to established protocol. Monitors workflow and makes necessary adjustment to complete work in an appropriate time frame.
• →Adheres to the Aurora Service Commitment, and the Power of Diversity in interactions with all internal and external customers.

Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including:

• Cytotechnologist (CT) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP BOC).

• Bachelor's Degree in Cytotechnology.

• Typically requires 3 years of experience in demonstrating proven expertise in cytology high complexity testing.

• Maintains patient confidentiality in and out of the workplace.
• Demonstrates a willingness to work a flexible schedule, which may include alternate site assignment.
• Maintains constructive and effective communication to enhance department performance.

• Must be able to operate all equipment essential in performing the job.
• Frequently lifts up to 10 lbs. Will occasionally be required to lift up to 50 lbs.
• Must be able to sit, stand, or walk the majority of the workday. Also required to lift and bend throughout.
• May be exposed to mechanical, electrical, chemical, explosive, radioactive and/or infectious agents.
• May be required to wear laboratory coats, gloves, gowns and eye and face protection as needed.
• Will be exposed to human blood and body fluids.
• Must be able to handle stressful situations in a calm and professional manner. May require occasional travel, therefore may be exposed to inclement weather and adverse road conditions.
• Must have ability to attend and complete required continuing education classes and credits.

Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.