Job summary
Job post source
This job is directly from Cystic Fibrosis Foundation
Job overview
The Scientist - Genome Editing role at the Cystic Fibrosis Foundation involves developing transformative genetic therapies for cystic fibrosis by leading genome editing research to correct CFTR gene mutations, impacting treatment options for people with cystic fibrosis.
Responsibilities and impact
The scientist will lead and coordinate research efforts, develop and improve protocols, manage lab work accuracy, collaborate across teams, maintain detailed records, and present findings internally and externally to support therapeutic development.
Compensation and benefits
The salary range is $122,500 to $153,000, varying by location and experience, with comprehensive benefits including medical, dental, vision coverage, life and disability insurance, retirement savings, paid vacation, sick leave, holidays, personal days, and work-life benefits.
Experience and skills
Candidates must have a Ph.D. with at least two years of relevant experience or a Master's with ten years of lab experience, strong gene editing skills especially with CRISPR/Cas and related technologies, excellent communication, collaboration, problem-solving, and organizational skills.
Career development
The position offers opportunities to participate in academic and industry collaborations and to initiate new projects, supporting continuous learning and professional growth within a mission-driven nonprofit environment.
Work environment and culture
The Foundation promotes a collaborative, inclusive, and mission-driven culture focused on excellence, innovation, and caring for people with cystic fibrosis and its employees, supporting diversity and work-life balance.
Company information
The Cystic Fibrosis Foundation is a leading nonprofit healthcare organization dedicated to curing cystic fibrosis through funding research, drug development, and specialized care, with a history of enabling nearly every CF drug available today.
Team overview
The genome editing scientist will join a team of experienced scientists working on gene editing approaches, collaborating with stem cell biology, genomics, and electrophysiology teams to develop and evaluate genetic therapies and cell models.
Job location and travel
The position requires commuting to the lab daily with occasional weekend work, access to reliable transportation, and the ability to work from home when travel is unsafe due to road conditions.
Application process
Applications are accepted on an ongoing basis with a minimum posting of five days; candidates are encouraged to apply promptly, with accommodations available for applicants with disabilities upon request.
Unique job features
This role is distinguished by its focus on innovative gene editing techniques including large DNA insertions and super exon strategies to treat cystic fibrosis, with opportunities to engage in cutting-edge collaborations and translational research.
Company overview
The Cystic Fibrosis Foundation is a nonprofit organization dedicated to funding research and drug development to find a cure for cystic fibrosis, a genetic disorder affecting the lungs and digestive system. They make money through donations, fundraising events, and partnerships with pharmaceutical companies. Founded in 1955, the Foundation has played a crucial role in advancing treatments and improving the quality of life for those with cystic fibrosis, including the development of breakthrough medications like Trikafta.
How to land this job
Position your resume to emphasize hands-on experience with genome editing technologies such as CRISPR/Cas systems, recombinases, and integrases, highlighting your ability to perform large gene insertions and work with human cell models relevant to cystic fibrosis research.
Highlight your collaborative skills and experience working across multidisciplinary teams, including contributions to experimental design, data analysis, and presentations, to align with the Foundation's value of working stronger together.
Apply through multiple platforms including the Cystic Fibrosis Foundation's official careers page, LinkedIn, and other job boards where the position is posted to maximize your chances of being noticed.
Connect with current employees in the genome editing or therapy lab divisions on LinkedIn; start conversations by referencing recent CF Foundation research breakthroughs or asking about their experience working on CFTR gene editing projects as ice breakers.
Optimize your resume for ATS by incorporating key phrases from the job description such as 'genome editing,' 'CRISPR/Cas,' 'large gene insertion,' 'primary human cell models,' and 'collaborative research,' ensuring your resume passes initial automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and find relevant LinkedIn contacts to network with, allowing you to focus more effectively on preparing for interviews and advancing your career.
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