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Remote Crispr Therapeutics Jobs (NOW HIRING)

Post-Doctoral Associate

Austin, MN ยท On-site +1

$62K - $72K/mo

Focus of Job Responsibilities Experimental Design and Therapeutic Evaluation 60% Conduct in vitro ... Target Validation and Molecular Engineering 20% Use shRNA/CRISPR gene-targeting approaches to ...

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 ...

Remote Crispr Therapeutics information

What is the difference between Remote Crispr Therapeutics vs Remote Molecular Biologist?

AspectRemote Crispr TherapeuticsRemote Molecular Biologist
Required credentialsAdvanced degrees in genetics, molecular biology, or related fields; experience with gene editing technologiesDegree in biology, biochemistry, or related fields; laboratory experience in molecular techniques
Work environmentResearch labs, biotech companies, or remote research settings focused on gene editingLaboratories, research institutions, biotech firms, with some remote opportunities
Employer and industry usageBiotech companies specializing in gene editing and therapeuticsResearch institutions, biotech firms, pharmaceutical companies

Remote Crispr Therapeutics roles focus on gene editing technologies like CRISPR, often requiring specialized biotech experience. Remote Molecular Biologist positions involve laboratory research in molecular techniques, with some remote options. Both roles are integral to biotech and research industries but differ in technical focus and work environment.

What are some common challenges faced when working remotely in a CRISPR therapeutics role, and how can they be addressed?

Working remotely in CRISPR therapeutics often involves navigating the complexities of virtual collaboration, particularly when coordinating experiments or sharing sensitive data with interdisciplinary teams. Communication can be challenging, especially when discussing intricate scientific concepts or troubleshooting experimental results. To address these challenges, remote professionals typically rely on robust digital collaboration platforms, regular video meetings, and clear documentation practices. Staying proactive about updates and maintaining open lines of communication with lab-based colleagues is essential for ensuring research continuity and data integrity.

What CRISPR company did Bill Gates invest in?

Bill Gates has invested in CRISPR companies such as Mammoth Biosciences and Editas Medicine, which focus on gene editing technologies. These investments reflect his interest in advancing biotech solutions for healthcare and disease treatment.

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

To thrive as a Remote CRISPR Therapeutics Specialist, you need a strong background in molecular biology, genetics, and gene-editing techniques, typically supported by an advanced degree in life sciences. Familiarity with CRISPR/Cas9 systems, bioinformatics tools, and laboratory information management systems (LIMS) is essential. Strong analytical thinking, attention to detail, and effective collaboration in virtual environments set standout professionals apart. These skills ensure precise gene-editing work, accurate data interpretation, and successful project outcomes in a remote research setting.

How much does CRISPR pay?

Salaries for CRISPR-related roles, such as research scientists or bioinformatics specialists, typically range from $70,000 to over $130,000 annually depending on experience, location, and level of expertise. Entry-level positions may start lower, while senior roles or those requiring specialized skills can command higher compensation.

What are Remote CRISPR Therapeutics jobs?

Remote CRISPR Therapeutics jobs are positions that allow professionals to work from home or any location outside the traditional workplace, focusing on gene-editing technologies like CRISPR. These roles can range from research and development to data analysis, project management, regulatory affairs, or scientific writing, all centered around CRISPR-based therapies. Remote positions typically require strong communication skills, proficiency in relevant scientific fields, and the ability to collaborate virtually with global teams. This flexibility enables companies to tap into a wider talent pool and allows employees to maintain a better work-life balance.

Does CRISPR Therapeutics have a future?

CRISPR Therapeutics is a leading company in gene editing technology, with ongoing research and development in therapies for genetic diseases. The company's focus on innovative CRISPR-based treatments suggests a strong future outlook within the biotech industry. Job roles in this field often require knowledge of molecular biology and genome editing tools, indicating continued growth opportunities for professionals in the sector.

Does Pfizer offer remote work?

Remote work policies at Pfizer vary by role and department, including positions related to CRISPR therapeutics. Many roles in research, development, and corporate functions may offer flexible or remote work options, especially for experienced professionals and those with digital collaboration tools. Job seekers should review specific job postings for remote work availability and requirements.
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What cities are hiring for Remote Crispr Therapeutics jobs? Cities with the most Remote Crispr Therapeutics job openings:
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Infographic showing various Remote Crispr Therapeutics job openings in the United States as of July 2026, with employment types broken down into 9% Locum Tenens, 20% Internship, 26% As Needed, 21% Full Time, 9% Part Time, and 15% Nights. Highlights an 67% Physical, 1% Hybrid, and 32% Remote job distribution.
Senior Director, Functional Genomics & Organoid Systems Biology

Senior Director, Functional Genomics & Organoid Systems Biology

Tempus

Chicago, IL โ€ข On-site, Remote

Full-time

PTO

Posted 3 days ago


Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are seeking an exceptional Senior Director, Functional Genomics & Organoid Systems Biology to lead and expand our patient-derived organoid (PDO) biology platform. This leader will drive the wet lab component of our systems biology team, and will help define how this experimental layer will combine with computational approaches and the massive multimodal Tempus data layer to unlock new biological insights. This leader will oversee a multidisciplinary team of scientists and research associates responsible for executing large-scale functional screens-including CRISPR-based genetic perturbation screens, drug sensitivity screens, single-cell and spatial technologies, and combination therapy studies-in clinically annotated patient-derived organoid models.

The successful candidate will define and drive the scientific vision for leveraging PDOs to validate hypotheses generated from Tempus' unique real-world clinico-genomic data assets. Working closely with computational scientists, machine learning researchers, translational scientists, and clinical teams, this individual will establish an integrated discovery engine that translates patient data into experimentally validated therapeutic opportunities.

This is a highly visible leadership role that combines scientific strategy, organizational leadership, platform development, and translational research to identify novel targets, biomarkers, and therapeutic strategies for cancer patients.

This position is based in Tempus' Chicago lab: hybrid or remote candidates will not be considered.

Key Responsibilities
  • Define and execute the long-term scientific strategy for functional screening and target discovery using patient-derived organoid models.

  • Establish a world-class organoid-based discovery platform capable of validating hypotheses generated from large-scale multimodal patient datasets.

  • Serve as a scientific thought leader internally and externally, representing the company through publications, presentations, and strategic collaborations.

  • Oversee the design, execution, and interpretation of large-scale CRISPR screening campaigns, including knockout, activation, interference, and pooled screening approaches.
  • Lead drug screening efforts across diverse PDO models to identify therapeutic sensitivities, resistance mechanisms, and rational drug combinations.

  • Drive development of next-generation functional assays incorporating co-culture systems, immune components, and emerging technologies.

  • Establish rigorous experimental standards, quality systems, and reproducible workflows across the screening platform.

  • Ensure efficient scaling of laboratory operations to support discovery and translational research objectives.

  • Partner closely with computational biology and data science teams to prioritize hypotheses arising from real-world patient data.
  • Create an iterative discovery framework in which computational predictions are experimentally tested and experimental findings inform subsequent computational analyses.

  • Collaborate with clinical, molecular profiling, and translational research teams to connect experimental findings with patient outcomes and therapeutic hypotheses.

  • Build, lead, and mentor a high-performing team of scientists, research associates, and laboratory personnel.
  • Foster a culture of scientific excellence, innovation, accountability, and collaboration.

  • Recruit top-tier talent across functional genomics, organoid biology, and translational oncology.

  • Establish clear goals, development plans, and performance expectations for team members.

  • Manage departmental budgets, resource allocation, and strategic planning.

Required Qualifications
  • PhD, MD, or MD/PhD in Cancer Biology, Molecular Biology, Genetics, Functional Genomics, Bioengineering, or a related discipline.

  • 8+ years of relevant industry and/or academic experience, including substantial leadership experience.

  • Deep expertise in cancer biology, functional genomics, and target discovery.

  • Demonstrated experience leading CRISPR-based screening programs and large-scale functional biology initiatives.

  • Hands-on experience with patient-derived organoids, ex vivo models, or other clinically relevant disease model systems.

  • Track record of translating biological insights into therapeutic hypotheses, biomarkers, or drug discovery programs.

  • Experience managing and mentoring multidisciplinary scientific teams.

  • Strong publication and/or patent record demonstrating scientific impact.

  • Excellent communication skills and ability to influence across scientific and executive stakeholders.

CHI: $190,000 - $270,000

The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.