Myeloid Therapeutics, Inc. Cambridge , MA 02138
Posted 2 weeks ago
Company Overview:
Myeloid Therapeutics is a clinical stage immunology company, engineering cutting-edge RNA technology to program immune cells to combat cancer and other deadly diseases. Myeloid is headquartered in Cambridge, MA. For additional information, please visit https://www.myeloidtx.com/ and follow us on LinkedIn and X/Twitter.
Position Summary:
Myeloid Therapeutics is seeking an innovation-driven Associate Director to join our RetroT Gene Editing team and contribute to the engineering and development of novel gene editing systems.
MyeloidTx has developed CRISPR-Enabled Autonomous Transposable Element (CREATE), a genome editing system that combines the programmability and precision of CRISPR/Cas9 with the RNA-mediated gene insertion capabilities of the human LINE1 (L1) element. CREATE represents a significant advancement in gene editing technology, establishing a new paradigm of RNA-based gene therapy.
We are seeking an Associate Director to enhance the CREATE technology, focusing on elevating editing efficiencies and broadening its application to disease-relevant primary cell types. This role offers the opportunity to lead a dedicated team within MyeloidTx, contributing to both internal research initiatives and vital external collaborations. The successful candidate will leverage their deep expertise in culture of primary hepatocytes and/or iPSC derived hepatocytes/neurons to contribute to optimization of delivery and gene editing efficiency. This is an opportunity for creative, outside-of-the box thinking and rapid learning and growth towards the development of a revolutionary gene editing technology.
Responsibilities:
Lead a dedicated team of scientists and research associates in optimizing CREATE system design, delivery, and editing efficiencies across various cell types
Design, produce, and refine RNA-based gene editing constructs by leveraging deep expertise in programmable DNA nucleases (Cas9, Cas12, etc.) and transposable elements
Develop and implement NGS-based assays to comprehensively evaluate editing outcomes, including efficiency, fidelity, and off-target effects
Spearhead a robust research plan built on well-controlled scientific experiments, documenting all planning and progress in an electronic lab notebook
Effectively communicate findings and conclusions to the broader scientific team, external collaborators, and at scientific conferences
Qualifications and Education:
Ph.D. in Genetics, Biochemistry, Molecular Biology or related disciplines with 3-5 years of industry experience.
Extensive knowledge and a strong track record in the design, characterization, and/or preclinical development of novel CRISPR and related genome-editing systems and/or mobile genetic elements.
In-depth expertise in qPCR, RT-qPCR and NGS sequencing for characterization of gene editing outcome are required.
Demonstrated ability to innovate and think outside-the-box, pushing the boundaries of gene editing technology.
Exceptional communication skills, with the ability to articulate complex scientific concepts in a clear and coherent manner.
Adept at managing multiple projects in a dynamic, fast-paced environment, prioritizing effectively to drive progress.
Track record of scientific innovation and thinking outside-of-the-box
Myeloid Therapeutics, Inc.