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Job No. 152642

  • Job Title:
  • Healthcare Principal Professional – Histotechnologist - 33122
  • Employer:
  • University of Colorado at Denver and Health Sciences Center
  • Location:
  • Aurora , CO
  • Posting Date:
  • 01-Apr-2024
  • Description:
  • Job Summary:

    This position requires a leader for the Pathology Shared Resource Tissue Microarray Core. In addition, this person will be responsible for operational oversight, supply management and ordering, and equipment acquisition and maintenance.

    Principal Professionals with special requirements for histology, large-scale clinical cohort Tissue Microarray (TMA) construction expertise, translational clinical laboratory supply management skills, and general laboratory supervision capabilities. Sectioning and staining for ongoing clinical research projects and clinical trials. Operational management and specialized procurement skills required for clinical research. Oversight and training of staff and students in the area of Tissue Micro Array development and lab operations.

    Tissue Micro Array Core: This person will serve as the subject matter expert of the Pathology Shared Resource (PSR) Tissue Micro Array Core. The PSR is an institution-wide facility that provides research and clinical trial services and is a Shared Resource for the University of Colorado Cancer Center (UCCC). The PSR leverages the clinical infrastructure of the Department of Pathology to provide a wide range of services including biorepository, histology, molecular pathology, cytogenetics, and management of the large Surgical Pathology Archive for clinical and research use.

    Clinical Trial and Research Support: The person in this function will work closely with clinical research teams at UCHealth, the Cancer Center, and the wider university to provide histology services for patient trial eligibility and correlative research objectives. The person in this position will also be responsible for procurement and microdissection of specific tissue/tumor lesions from patient tissue to be used for molecular analysis of nucleic acids (RNA/DNA) including, but not limited to, mutation analysis, RNAseq and whole genome/exon sequencing.

    Operational management: The PSR, specifically the person fulfilling this role, is responsible for sourcing the consumables needed to collect, process, and analyze clinical research biospecimens from patients (including specialized vacutainers, containers, reagents, etc.). In this challenging environment, the sourcing of the critical supplies required for procurement, processing, and analysis of biospecimens is both demanding and vital, requiring a person with demonstrated capabilities in this area to keep the PSR fully operational and prevent interruption of ongoing clinical trials and research studies.

    Professional Field: Clinical Translational Laboratory. The PSR manages a diverse and extensive longitudinal collection of clinical research material including the Department of Pathology surgical Pathology Archive that contains clinical specimens from diagnostic and surgical procedures performed at the University Hospital. These clinical materials, together with specimens collected for research and clinical materials retrieved form external institutions, form the basis of many clinical research studies supported by the PSR and are also the source material for the creation of TMAs. The organization and creation of TMAs encompassing the full spectrum of disease states, treatment types, patient demographics, and clinical outcomes supports research into the mechanisms of human disease, efficacy of interventions, clinical trials, and new technologies. The person in this position will provide subject matter expertise to diverse teams of investigators, statisticians, and technical staff to successfully develop patient and specimen cohorts and create TMAs that can be studied utilizing high-throughput analysis platforms (such as Vectra and MIBI). The person in this position will be responsible for communication and coordination with our partner Shared Resources for downstream analysis

    Key Responsibilities:

    Operation of TMA core: 40%

    Construction of specialized human subject TMAs representative of disease progression and epidemiology which support clinical research projects and development of new analysis technologies. Clinical cohort TMAs will be used in downstream applications including, but not limited to, high throughput platforms such as Vectra and MIBI.
    TMA planning, organization, and management
    Data collection and management
    TMA construction
    Histology services: 50%

    Clinical Research histology (FFPE and frozen) for patient-oriented research and clinical trials. Sectioning and preparation of tissues and other materials required for patients to enroll in clinical trials, receive experimental treatments and for correlative research. Tissue sectioning for pathologist evaluation to determine eligibility of patients for clinical trials.
    Histology service for research projects and TMA projects
    Dissection of tumor lesions from FFPE specimens for nucleic acid sequencing. This genetic data is used for development and validation of therapeutics targeted to specific demographics and disease states. Genetic data is also used for discovery studies to find specific germline or somatic mutations or RNA expression profiles associated with disease onset, progression, and prognosis.
    Management of equipment, supplies, and ordering – 10%

    Operational oversight of a clinical translational laboratory with the complex needs and protocols inherent in the clinical research environment (including adherence to specialized protocols, management of supply lifecycle and supply chain management in unprecedented situations).
    Management of ordering software, training and onboarding of team members.
    Ongoing surveillance of supply chain environment. Extensive networking with suppliers. Requirement to maintain productive relationships with vendors, monitor product quality, origin, value, availability, suitability, and compliance with an array of clinical protocols.
    Management of space changes and equipment movement including equipment certification, green tagging and disposals. Planning of replacement and new equipment purchases.
    Why Join Us:

    Welcome to the Department of Pathology of the University of Colorado, Anschutz Medical Campus. The Department has grown substantially in the past 15 years, from 40 to 120 faculty in parallel with the remarkable growth of our hospital-based affiliates as well as the city and county of Denver. Our work is value driven and focused on scientific investigation, lifelong learning, and a balance of personal and professional values. In addition to a vibrant and highly competitive residency program with 25 positions, we offer 9 fellowships and participate in numerous graduate schools and the MD/PhD program of the CU School of Medicine. Our faculty and staff are diverse, and gender balanced, with women comprising 50% of our residents, Assistant, Associate and Full Professors (including those with tenure).

    Supervision Received: Adrie van Bokhoven, PhD, Co-Director Pathology Shared Resource

    Supervision Exercised: The individual is responsible for the supervision and evaluation of the PSR team members and students.
  •  Contact information:
  • University of Colorado at Denver and Health Sciences Center
  • Aurora, CO 80217
  • United States
  • Employer's Website:
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