Oncology Pathology Assist - 2nd Shift

Requirements

• Bachelor's degree, or higher, with certification as a Histology Technologist by the American Society of Clinical Pathology (ASCP), or equivalent board, is required.
• Minimum of 5 years of experience in anatomic pathology including extensive knowledge of solid tumor pathology.
• KNOWLEDGE, SKILLS, AND ABILITIES:
• Ability to accurately understand and convey information found in anatomic pathology reports to team members for a wide variety of solid tumors, including but not limited to lung, colon, and breast cancer.
• Ability to identify potential diagnostic sample(s) that will ensure successful testing.
• Ability to communicate effectively with team members and referring pathology laboratories.
• Ability to build relationships with referring pathology laboratories.
• Detail oriented. Ability to think broadly about the importance of clinical information and to work independently.
• OUR OPPORTUNITY

Benefits

Additional Information

POSITION SUMMARY: This position supports our 2nd Shift operations, with a scheduled start time of 12:00 PM PST. The Oncology Pathology Assistant (Histology Technologist) provides assistance to the Signatera team as a subject matter expert for review of clinical pathology reports. The Histology technologist will assist the medical and customer service teams with acquisition of appropriate specimens for minimal residual disease (MRD) testing in oncology. PRIMARY RESPONSIBILITIES: Assist the medical and customer service teams with the interpretation of oncology pathology reports to identify optimal samples to request when initial FFPE blocks or slides are inadequate for testing. Read and ensure accurate curation of clinical history, diagnosis, progress notes, and specimen information is entered into the Signatera sample database. Assist with devising strategies to stratify data for retrieval from the Signatera sample database and other databases as necessary. Maintain proficiency with and help organize diagnostic data according to pertinent WHO guidelines. Serve as subject matter expert to the Laboratory Director, Genetic Counseling, Customer Experience, Sales, and Clinical Trial teams for pathology reports. Assist in the identification and alert the Laboratory Director when samples may have been collected at suboptimal timepoints and/or fixative conditions. Assist Genetic Counseling and Customer Experience teams in identification and procurement of optimal additional samples, as necessary. Provide professional support for the Clinical Trial team through accurate and organized data transfer. Performs other duties as assigned.

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Company Intel

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