New

Cell Therapy Correlative Study Specialist, CICET

Columbia University
United States, New York, New York
Jan 29, 2026
Job Type: Officer of Administration Regular/Temporary: Regular Hours Per Week: 35 Salary Range: $66,300 - $85,000 The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. Position Summary The Columbia Initiative for Cell Engineering and Therapy (CICET) Cell Therapy Correlative Study Specialist will support the translational and clinical research efforts for investigational cell therapy programs. Reporting to the Director of the CICET Translational Laboratory, this role works closely with the CICET Clinical Trials Management and CICET GMP/QC teams as well as external collaborators to support the design, development, and execution of correlative study assays. The Correlative Study Specialist plays a critical role in generating high-quality, reproducible data from patient-derived and healthy donor samples to advance mechanistic understanding of cell therapy products and to support clinical development, biomarker discovery, and translational research objectives. Responsibilities The Cell Therapy Correlative Study Specialist is responsible for coordinating, processing, analyzing, and documenting clinical samples collected in company-sponsored and investigator-initiated cell therapy trials. In collaboration with the CICET Translational Laboratory manager, this role supports day-to-day laboratory operations, performs correlative and immune-monitoring assays, maintains laboratory organization and inventory, and interfaces closely with the CICET clinical trial management team to ensure timely, compliant, high-quality translational research outputs. Correlative Assay Execution and Sample Management * Coordinate timely transfer, tracking, receipt, and documentation of patient samples from CUIMC in collaboration with the CICET Clinical Trials Management staff to ensure sample integrity and protocol compliance * Process, aliquot, and store blood and bone marrow specimens in accordance with study protocols and laboratory SOPs * Perform immune cell phenotyping using multiparameter flow cytometry * Conduct cytokine and gene expression analyses using PCR-based methodologies (e.g., qPCR) * Support single-cell genomics and immune profiling assays as required by study design Laboratory Operations and Data Integrity * Maintain accurate laboratory records, including sample tracking, experimental documentation, and data entry * Ensure proper labeling, storage, and inventory control of clinical samples and laboratory reagents * Support laboratory organization, cleanliness, and readiness for ongoing translational studies * Adhere to institutional biosafety requirements and data integrity standards Collaboration and Communication * Interface regularly with the Director and laboratory management to align correlative study activities with program priorities * Collaborate with Clinical Trials Management to ensure proper sample logistics and protocol adherence * Work closely with external collaborators, GMP/QC, and research teams to support translational data needs Additional Responsibilities * Assist with onboarding and training of new laboratory staff or trainees as needed * Support continuous improvement of translational laboratory workflows and assay execution * Participate in team meetings and contribute to cross-functional translational planning efforts Minimum Qualifications * Bachelor's degree in Biology, Immunology, Molecular Biology, or related life science discipline * Basic experience in processing and culturing mammalian primary cells and cell lines * Hands-on experience in multi-parameter flow cytometry (sample processing, staining, acquisition, and analysis) * Experience and training in handling human blood, serum, and bone marrow samples * Strong organizational skills with attention to detail and data accuracy * Ability to work independently and collaboratively in a multidisciplinary research environment * Effective written and verbal communication skills * Knowledge of Microsoft Office Suite and database systems Preferred Qualifications * Master's degree in a related life science discipline * Minimum of 1-2 years of relevant laboratory experience supporting correlative studies for cell or gene therapy clinical trials, preferably in immunology-focused research * Hands-on experience with PCR-based assays and in spectral flow cytometry, including flow sorting * Hands-on experience in sample preparation for single-cell genomics assays * Familiarity with immune monitoring, biomarker development, or translational assay workflows Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.