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Publication Programs: Platform

Genome Engineered Hematopoietic Transplants for the Treatment of AML

Keystone Symposia – 2025 – Oral Presentation […]

Read More… from Genome Engineered Hematopoietic Transplants for the Treatment of AML

Clinical Holds for Cell and Gene Therapy Trials: Risks, Impact, and Lessons Learned

Molecular Therapy: Methods & Clinical Development – Review […]

Read More… from Clinical Holds for Cell and Gene Therapy Trials: Risks, Impact, and Lessons Learned

Development of a Gene Edited Next-Generation Hematopoietic Cell Transplant to Enable Acute Myeloid Leukemia Treatment by Solving Off-Tumor Toxicity

Molecular Therapy: Methods & Clinical Development – Peer-Reviewed Manuscript […]

Read More… from Development of a Gene Edited Next-Generation Hematopoietic Cell Transplant to Enable Acute Myeloid Leukemia Treatment by Solving Off-Tumor Toxicity

Gene Editing and Immunotherapeutic Targeting of ADGRE2/EMR2 to Enable Combinatorial Targeting in Acute Myeloid Leukemia (AML)

ASGCT – 2023 – Poster Presentation 618 […]

Read More… from Gene Editing and Immunotherapeutic Targeting of ADGRE2/EMR2 to Enable Combinatorial Targeting in Acute Myeloid Leukemia (AML)

Translocation Detection and Quantification Workflow to Characterize CRISPR-Cas Multiplex Edited Hematopoietic Stem and Progenitor Cells (HSPCs)

Keystone Symposia – 2023 – Poster Presentation 3527 […]

Read More… from Translocation Detection and Quantification Workflow to Characterize CRISPR-Cas Multiplex Edited Hematopoietic Stem and Progenitor Cells (HSPCs)

Leveraging Human Genetics To Advance Cell Therapies For Treatment Of Blood Cancers

Cell & Gene – White Paper […]

Read More… from Leveraging Human Genetics To Advance Cell Therapies For Treatment Of Blood Cancers

A Machine Learning Approach Incorporating Germline Information Improves Genotyping of CRISPR-Cas9 Gene Editing Events at Single Cell Resolution

Rocky Conference – 2022 – Poster Presentation 71 […]

Read More… from A Machine Learning Approach Incorporating Germline Information Improves Genotyping of CRISPR-Cas9 Gene Editing Events at Single Cell Resolution

Efficient Multiplex Gene Editing of CD33 and CLL-1 in Human Hematopoietic Stem Cells Enables the Potential of Next-Generation Transplants for AML Treatment

ASH – 2022 – Poster Presentation 4587 […]

Read More… from Efficient Multiplex Gene Editing of CD33 and CLL-1 in Human Hematopoietic Stem Cells Enables the Potential of Next-Generation Transplants for AML Treatment

Functional Validation of Single Domain Antibody-Derived CD33 Specific CAR-T Cells for the Treatment of Acute Myeloid Leukemia

SITC – 2022 – Poster Presentation P334 […]

Read More… from Functional Validation of Single Domain Antibody-Derived CD33 Specific CAR-T Cells for the Treatment of Acute Myeloid Leukemia

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All employment opportunities at Vor Biopharma are managed by our in-house Human Resources Department. Therefore, agency staff and independent recruiters must contact the Human Resources Department directly in order to present candidates or inquire about openings. Please do not contact other Vor Bipharma employees. Your ability to comply with this request will significantly impact any decision we may make about doing business with you.

Please understand that we do not accept unsolicited resumes from any source other than from the candidates themselves. Any agency or independent recruiter must have a signed copy of our agency agreement before presenting candidates. Submission of unsolicited resumes without our signed agreement will not create any implied obligation on our part.

If you wish to be considered for the presentation of candidates, please contact us through careers@vorbio.com. Attach your contact information, your area of specialty, and any marketing information you wish to provide. Someone from the Human Resources Department will contact you directly if there is a business need for your services.