Laboratory Technician

Laboratory Technician

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Job Description

  • Perform technical duties related to the supporting of the cell and molecular microbiology protocols.
  • Maintain complete, accurate, legible, neat, organized, up-to-date records/logs/files,
  • Assure the accuracy of all tests performed by adhering to the Laboratory’s Standard Operating Procedures
  • Perform routine and advanced equipment maintenance
  • Contribute to the upkeep and safety of the Laboratory and assures a clean, safe, adequately supplied work area
  • Participate in the laboratory inventory program that provides adequate inventories of reagents and supplies
  • Create and help maintain an environment that emphasizes safety following New York State DOH, Joint Commission, OSHA and CLIA regulations
  • Provide direction, training, and feedback on routine laboratory procedures, as assigned
  • Maintain and upkeep of REDCap, Microsoft Access, and Microsoft Excel databases for several clinical research projects
  • DNA extractions from blood and saliva specimens
  • Multiplex monochrome quantitative PCR assays for telomere length screening
  • Create sample requests to institutional sample banks including the Center for Molecular Oncology
  • Coordinate the pickup of samples from the Integrated Genomics Operation
  • Handle regulatory approved requests from other laboratories at MSKCC to aliquot samples from our cryostorage
  • Organize and maintain a large cohort of blood specimens
  • Aggregate and organize datasets for multi-institutional research projects
  • Lead the efforts to compile phenotypic data for samples sent for genomic sequencing and analysis
  • Coordinate clinical sample drop-offs with other labs, update sample databases, and store samples safely and appropriately
  • Prepare genomic DNA samples for shipment, including pulling samples, performing quality control assays, create dilutions, compile sample manifests, and prepare plates or tubes for shipment
  • Package and ship samples, including nucleic acid, biospecimens, slides, and tumor blocks to collaborating institutions
  • Independently coordinate sample shipments with external collaborators
  • Perform routine and advanced equipment maintenance
  • Participate in the laboratory inventory program that provides adequate inventories of reagents and supplies
  • Maintain complete, accurate, legible, neat, organized, up-to-date records/logs/files,
  • Assure the accuracy of all tests performed by adhering to the Laboratory’s Standard Operating Procedures
  • Contribute to the upkeep and safety of the Laboratory and assures a clean, safe, adequately supplied work area
  • Provide direction, training, and feedback on routine laboratory procedures, as assigned
  • Screen patient records and databases to determine patient eligibility for studies;
  • Contribute to development and maintenance of study databases;
  • Support the PIs and study team as needed for data analysis and relevant project duties;
  • Perform data entry and conduct regular audits to ensure data accuracy and integrity;
  • Present regular updates at lab meetings
  • Contribute to scientific presentations and publications;
  • Perform literature searches and other tasks as needed.
  • Be responsible for data collection including utilizing appropriate methodologies to collect human subject information for a research project, database and/or protocol (research study) by reviewing patient charts, existing databases, and other sources within a specified timeframe.
  • Coordinate data pulls from multiple sources by leveraging institutional query tools as well as the MSKCC Dataline team
  • Inventories and orders supplies and reagents to ensure adequate stock
  • Properly dispose hazardous waste
  • Assist with instrumentation maintenance
  • Coordinate sample transfers between the Clinical Genetics Service and the Clinical Genetics Research Laboratory
  • Oversee the work of volunteers, interns, or laboratory aids as directed; provide guidance and feedback; report performance and progress

Regulatory

  • Coordinate the establishment of contracts (MTA, DTA, DUA, etc.) between MSKCC and external collaborators with in-house attorneys and the eContracts platform
  • Complete continuing review reports for IRB compliance for ongoing research studies
  • Enroll patients in clinical research studies by providing study-specific information and obtaining informed consent to participate
  • Write and amend research protocols for IRB submission