Indianapolis, Indiana
LabCorp
Sign-on Bonus $7,500
The Histotechnologist is accountable for the histology handling/storing of precious clinical trial specimens. The Histotechnologist supports the various teams of the Specimen Management Center and is a liaison between Specimen Management and others departments. The Histotechnologist will actively liaise with the CCLS project management team, Investigator Support Team and client to resolve and clarify questions and/ or issues related to management and preparation of the histology samples.
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 .
Essential Job Duties:
Specific department duties as set forth in the task list and/or department training checklists including but not limited to:
Utilize knowledge and experience with histology samples to maintain proper storage conditions and facilitate accessioning of blocks and slides (stained and unstained).
Routine decalcification, processing, embedding, microtomy and re-embedding of human tissue specimens from patients enrolled in clinical trials.
Perform routine, special stains, and advanced staining assays according to SOPs, protocols, and in line with global and regional regulatory requirements.
Perform slide scanning as required and according to protocols.
Ensure that Special Handling specimens are picked up from the appropriate area, sorted, accessioned, pre-scanned and registered into the appropriate temperature bins in a timely fashion.
Generation and application of specialized labels to include aliquot and/or mini labels with client specific elements.
General duties including but not limited to:
Resolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved.
Prepare workstation, instrumentation and maintenance on instruments and/or equipment daily, weekly, monthly, quarterly and annually. Ability to adequately maintain accurate records and both adhere to Standard Operating Procedures:
o Calibrate instruments, verification of temperature, and logging of data as required.
o Ensure that maintenance is performed and documented according to SOP.
o Perform basic instrument and/or equipment troubleshooting.
o Document corrective actions for unusual occurrences.
o Notify management when an instrument and/or equipment does not meet specifications.
o Ability to use different application software.
o Document quality control results.
o Perform proficiency testing survey as patient specimens.
Reagents, material and supplies monitoring:
o Order, receive, open and place in service all reagents/material according to SOPs.
o Document implementation of new reagents/material according to SOPs.
o Perform lot-to-lot comparison according to SOPS.
o Perform inventory and checks of reagents/material.
Adheres to all company policies and procedures and performs all departmental and interdepartmental SOP’s as written.
Adheres to safety and occupational health policies and standards.
Training
– Individual is responsible for maintaining his/her complete up-to-date training file, and is accountable for correcting any deficiencies found in his/her training file.
– Individual is responsible for ensuring he/she is trained and training is documented prior to perform a task.
– Individual successfully completes, as scheduled, competency assessment, and ensures competency testing documentation is provided to management for review.
– May assist in training of new employees and follow-up to ensure training is understood.
– Generates an appropriate audit trail of all activities and maintains own training file and required documentation.
Education/Qualifications/Certifications and Licenses
Individual must qualify as testing personnel under the following CLIA 1988 and New York State Department of Health requirements:
OR
OR
OR
HT (ASCP) certification or a minimum of 1 year experience
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility .
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