Everlum Bio is a personalized medicine company focused on creating treatments for people with rare diseases. We are happy to have celebrated three recent successes. We have designed and demonstrated the effectiveness of an Antisense-Oligos (ASO) to help HNRNPH2 (To Cure A Rose). We have a proof of concept gene therapy for two families with children suffering from a lysosomal storage disorder (LSD). Finally, we found a shelved drug that we are currently working to repurpose for a child with another LSD. We are on a mission to take these successes, and so many more, to the rare community. These are exciting times at Everlum and we are hiring.
Requirements
Minimum of 5 years of experience in a scientific research role
Strong background in molecular biology and genetics
Experience with stem cell-based model systems
Proficiency in cell culture techniques
Expertise in assay development and optimization
Ph.D. in a related field
Attention to detail and strong analytical skills
Ability to work independently and in a collaborative team environment
Full Job Description
We are seeking to bring induced pluripotent stem cell (iPSC) reprogramming and CRISPR-Cas9 mutagenesis capabilities in-house. By doing so, we aim to improve the timelines and costs associated with these critical processes. This strategic move will enable us to achieve faster turnaround times, reduce expenses and ensure higher efficiency and precision, ultimately benefiting the rare disease community we serve. In-house CRISPR mutagenesis capabilities will allow us to perform gene editing with greater accuracy and speed, advancing our ability to develop and test new therapies. These advancements will not only streamline our research and development processes, but also significantly lower the costs associated with these technologies. The savings and efficiencies gained will be passed on to the rare disease community, helping us deliver innovative treatments more quickly and affordably. Our commitment to improving the quality and accessibility of preclinical research drives this initiative. By controlling these processes internally, we reaffirm our dedication to providing timely, cost-effective solutions for our rare patients.
Responsibilities
Hands-on experience with IPSC reprogramming and CRISPR mutagenesis
Development of therapies to address patients' rare diseases
Leading scientific research projects and initiatives
Developing and implementing scientific strategies
Managing a team of scientists and researchers
Collaborating with other departments and external partners
Ensuring compliance with regulatory standards
Overseeing the publication of scientific papers and reports
Securing funding and managing budgets for scientific projects
Why Join Us
Innovative Environment: Be part of a cutting-edge science team dedicated to pioneering treatments for rare diseases
Professional Growth: Opportunities for continued education, research, and professional development
Impactful Work: Make a significant difference in the lives of children and their families by providing hope and improving health outcomes
Supportive Community: Work within a supportive and collaborative environment that values compassion, excellence, and patient-centered care
Benefits
Paid vacation
Paid Holidays
Healthcare plan
Dental Coverage
Seniority level
Director
Employment type
Full-time
Job function
Research
Industries
Primary and Secondary Education and Non-profit Organizations
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