обновлено 5 дней назад
Scientist (Cell Therapy)
96 267 - 126 351$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Scientist (Cell Therapy) (Immunology/Oncology): Developing next-generation in-vivo CAR-T and cell therapy technologies through immune-cell analytics, viral-vector engineering, and solid-tumor models with an accent on advanced flow cytometry, lentivirus characterization, and functional assays. Focus on designing in-vitro and in-vivo studies, measuring transduction and vector copy number, and delivering organized research data under GLP and EHS requirements.
Location: Onsite in Philadelphia, Pennsylvania, United States
Base pay: $96,267–$126,351 USD per year, plus performance-based bonus and/or equity for eligible roles.
Company
Global biotechnology company developing cell and gene therapies, including CAR-T, TCR-T, NK-cell, and in-vivo cell therapy platforms for cancer and autoimmune diseases.
What you will do
- Design and optimize research studies for next-generation in-vivo CAR-T and cell therapy approaches.
- Identify novel solutions to in-vivo cell therapy challenges through literature analysis and project formation.
- Isolate immune cells from donor or patient blood and evaluate engineered CAR viruses using in-vitro assays and in-vivo mouse models.
- Perform cell culture, transfection, flow cytometry, and cell-based functional assays for solid-tumor research.
- Package, titer, and characterize engineered viruses using protein, PCR, flow-based, and vector-copy-number assays.
- Manage research data in an organized manner, present findings to internal and external audiences, and maintain GLP and EHS compliance.
Requirements
- PhD in immunology or a related discipline.
- At least 2 years of experience in cell and gene therapy; in-vivo CAR-T experience is preferred.
- Advanced experience with immune-cell analytics, multiparameter flow cytometry, cytotoxicity assays, and cytokine-release ELISA/MSD multiplex assays.
- Experience with lentivirus production, titration, transduction, and particle characterization using molecular and flow-based assays.
- Knowledge of immunology, immunotherapy, molecular biology, cellular biology, modified viral vectors, and gene-delivery technologies such as LVV, VLP, or LNP.
- Applicants must be authorized to work in the United States; employment eligibility is verified through Form I-9 and E-Verify.
Nice to have
- Experience with solid-tumor models and in-vivo cell-specific gene delivery.
- Publications or patents demonstrating research productivity.
- Deep understanding of solid-tumor models.
Culture & Benefits
- Collaborative, fast-paced biotechnology research environment with independent project ownership.
- Medical, dental, and vision insurance and a 401(k) plan with company match.
- Eight weeks of paid parental leave after three months of employment.
- Paid vacation, personal and sick time, floating holidays, and company holidays.
- Additional disability, life, legal, commuter, family-care, wellness, and flexible spending benefits.
- Benefits are available exclusively to permanent full-time employees; contractors are not eligible.
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