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Remote Crispr Genome Editing Jobs (NOW HIRING)

... editing and modification) from diverse next-generation sequencing assays (Illumina, Ion Torrent, Pacific Biosciences; targeted panels, whole-exome sequencing, whole-genome sequencing, RNA-Seq; bulk ...

We continue to invest time, money and energy into making our onsite, hybrid and remote work ... CRISPR screens). * Define internal standards for validation of target discovery methods, including ...

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Remote Crispr Genome Editing information

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$45K

$83.1K

$157.5K

How much do remote crispr genome editing jobs pay per year?

As of Jun 10, 2026, the average yearly pay for remote crispr genome editing in the United States is $83,148.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $92,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote CRISPR Genome Editing Specialist, and why are they important?

To thrive as a Remote CRISPR Genome Editing Specialist, you need a solid background in molecular biology, genetics, and bioinformatics, typically supported by an advanced degree in a life science field. Proficiency with gene-editing tools (like CRISPR-Cas9), laboratory data analysis software, and cloud-based collaboration platforms is essential. Strong attention to detail, problem-solving abilities, and effective remote communication skills help set top candidates apart. These competencies ensure precise genome editing, accurate data interpretation, and seamless collaboration in a distributed research environment.

What is the difference between Remote Crispr Genome Editing vs Remote Molecular Biologist?

AspectRemote Crispr Genome EditingRemote Molecular Biologist
Required CredentialsAdvanced degrees in genetics, molecular biology, or related fields; specialized training in CRISPR techniquesDegree in biology, biochemistry, or related fields; some roles require lab experience
Work EnvironmentPrimarily laboratory-based with remote collaboration; focus on gene editing projectsResearch labs, data analysis, and remote collaboration on biological studies
Industry UsageBiotech, pharmaceutical, research institutionsAcademic, biotech, research organizations

Remote Crispr Genome Editing specialists focus on gene editing techniques using CRISPR technology, often requiring specialized training and working on cutting-edge genetic modification projects. Remote Molecular Biologists conduct broader biological research, including data analysis and lab work, with less emphasis on specific gene editing skills. Both roles are vital in biotech and research sectors but differ in technical focus and daily tasks.

What are some common challenges faced when working remotely in CRISPR genome editing roles?

Remote CRISPR genome editing professionals often face challenges related to limited access to laboratory facilities and hands-on experimentation. Collaboration can also be more complex, as coordinating with wet-lab teams requires clear communication and effective digital tools. However, many remote roles focus on data analysis, experimental design, or bioinformatics, allowing for meaningful contributions from afar. Regular virtual meetings and cloud-based data sharing are essential for staying aligned with the team and project goals.

What is remote CRISPR genome editing?

Remote CRISPR genome editing refers to the ability to design, initiate, or monitor genome editing experiments using CRISPR technology from a location outside of the laboratory, often via digital platforms and cloud-based bioinformatics tools. Scientists can remotely program experiments, analyze data, or even control laboratory equipment using specialized software. This approach increases accessibility, collaboration, and efficiency in research while maintaining rigorous standards for data security and experiment reproducibility.
More about Remote Crispr Genome Editing jobs
What cities are hiring for Remote Crispr Genome Editing jobs? Cities with the most Remote Crispr Genome Editing job openings:
What are the most commonly searched types of Crispr Genome Editing jobs? The most popular types of Crispr Genome Editing jobs are:
What states have the most Remote Crispr Genome Editing jobs? States with the most job openings for Remote Crispr Genome Editing jobs include:
Infographic showing various Remote Crispr Genome Editing job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $83,148 per year, or $40 per hour.
Director, Medical Communications

Director, Medical Communications

Intellia Therapeutics

Cambridge, MA • Remote

Full-time

Posted 4 days ago


Job description

Why Join Intellia?

Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.

Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.

We wantall ofour people to go beyond what is possible. We aren't constrained by typical end rails, and we aren't out to just "treat" people. We're all in this for something more. We're driven to cure and motivated for change. Just imagine the possibilities of what we can do together.

How You Will Achieve More:

The Director of Medical Communications will support the development and implementation of the Global Medical Communications and Publication plans for Medical Affairs. The Director of Medical Communications is responsible for ensuring that education and data gaps are addressed with strategic medical communication and publications to communicate scientific and clinical information to both internal and external stakeholders.

Responsibilities:

  • Strategically develop, lead and complete the Medical Communication and Publication Plans for assigned programs/therapeutic areas, ensuring robust strategic planning, tactical planning and implementation in alignment with global Medical Affairs objectives and initiatives
  • Maintain and execute Publication Plans for clinical and HEOR publications for assigned programs/therapeutic while leading a Publications Working Group (PWG) to ensure high quality and timely achievement of landmarks and deliverables
  • Develop medical education initiatives to fill external educational gaps including company-sponsored symposia, medical congress booths, and digital medical education and lead materials through the Medical/Legal/Regulatory review process
  • Lead the development and maintenance of scientific platform, scientific lexicon, Field Medical resources, advisory boards/round tables and other medical education content support for assigned programs/therapeutic areas, in collaboration with the program Medical Affairs Lead(s) and vendors; ensure medical accuracy and appropriate review/approval
  • Build effective partnerships with all stakeholders, including supported programs' Medical Program Leads, R&D Program Leads, HEOR Program Leads, Statistical Program Leads, IP, and Legal
  • Provide medical communications vendor oversight and project management, including budget management
  • Critically review/edit sophisticated medical communication and publication documents for quality, compliance and scientific integrity
  • Deliver innovative medical communication and publication solutions while ensuring fair balance and integrity
  • Ensure compliance with regulatory requirements as well as industry guidelines and Intellia policies

About You:

  • Excellent written and oral communication skills
  • Strong organizational skills and attention to detail
  • Time management skills with a proven ability to meet deadlines
  • Critical thinking with an innovative mindset required
  • Tight-knit collaboration and stakeholder management
  • Project management and vendor management skills
  • Self-starter with the ability to work collaboratively and the desire to work on a cross functional team
  • Strong analytical and problem-solving skills
  • Understanding of pharmaceutical clinical development and product life-cycle management
  • Proficient in Microsoft Word, PowerPoint, Excel, and technologically savvy
  • Willingness to travel (role anticipated to have about ~10-15% travel component)
  • Doctoral degree (Ph.D., PharmD) in a scientific discipline strongly preferred
  • Minimum of 5-7+ years of experience in medical writing, medical publications, and/or communications
  • Certification as a Medical Publication Professional (CMPP) is highly desirable
  • Ability to sit or stand for multiple hours at a computer
  • Manual dexterity for keyboarding; may include repetitive movements

#LI-Remote

EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down.

The base salary for this position is expected to range between $221,603.00 - $270,848.00 USD per year.

The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors.

Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company's discretion.

For more information about Intellia's benefits, please click here.