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Crispr Scientist Jobs (NOW HIRING)

Bristol Myers Squibb

Principal Scientist

San Diego, CA · On-site

As a key scientific leader, you will drive genome engineering, target validation, and mechanism of ... Apply deep expertise in CRISPR/Cas9 (KO/KI/Activation), non-viral transposases, and lentiviral ...

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Crispr Scientist information

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$50.5K

$130.1K

$174K

How much do crispr scientist jobs pay per year?

As of Jul 14, 2026, the average yearly pay for crispr scientist in the United States is $130,117.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,500.00 and $173,000.00 per year, depending on experience, location, and employer.

What biology jobs pay over $100k?

In the field of biology, roles such as senior research scientists, biotech project managers, and regulatory affairs directors often have salaries exceeding $100,000. These positions typically require advanced degrees, specialized skills, and experience in areas like genetics, molecular biology, or bioinformatics.

What does a CRISPR scientist do?

A CRISPR scientist researches and develops applications using CRISPR gene-editing technology. Their work involves designing experiments to modify genetic material in cells or organisms, analyzing results, and ensuring the accuracy and safety of genetic edits. CRISPR scientists may work in academic, medical, or biotechnology settings, contributing to advancements in medicine, agriculture, and biological research. They often collaborate with other scientists to explore new therapeutic approaches or improve crop traits.

What degree do I need to work with CRISPR?

A CRISPR scientist typically needs at least a bachelor's degree in a relevant field such as molecular biology, genetics, biochemistry, or biotechnology. Advanced roles often require a master's or Ph.D. with experience in gene editing techniques, laboratory skills, and familiarity with CRISPR tools and protocols.

What are some common challenges faced by a CRISPR Scientist when designing gene-editing experiments?

CRISPR Scientists often encounter challenges such as minimizing off-target effects, optimizing guide RNA design, and ensuring efficient delivery of editing components to target cells. Additionally, troubleshooting unexpected cellular responses and verifying precise genome edits can be time-consuming and require meticulous planning. Collaboration with bioinformaticians and molecular biologists is usually essential to overcome these obstacles and achieve robust, reproducible results.

Does CRISPR have a future?

CRISPR technology is expected to have a significant future in genetic research and medicine, creating opportunities for CRISPR scientists to develop gene editing therapies and improve disease treatments. As the field advances, roles for professionals skilled in molecular biology, bioinformatics, and laboratory techniques are likely to grow. Staying current with regulatory developments and ethical considerations is also important for CRISPR scientists.

How much does a CRISPR scientist make?

A CRISPR scientist's salary varies based on experience, education, and location, but typically ranges from $70,000 to over $130,000 annually. Senior roles or those with specialized skills in gene editing and laboratory techniques can earn higher salaries, especially in biotech or pharmaceutical industries.

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

To thrive as a CRISPR Scientist, you need a strong background in molecular biology, genetics, and genome editing, typically supported by an advanced degree such as a PhD in a relevant field. Familiarity with CRISPR-Cas9 technologies, gene editing software, cell culture techniques, and laboratory information management systems (LIMS) is essential. Attention to detail, critical thinking, and effective collaboration are crucial soft skills for designing experiments and interpreting complex data. These competencies are vital for advancing precise gene-editing research and ensuring rigorous, reproducible scientific outcomes.

What is the difference between Crispr Scientist vs Gene Editing Researcher?

AspectCrispr ScientistGene Editing Researcher
CredentialsAdvanced degrees in molecular biology, genetics, or related fields; experience with CRISPR technologySimilar credentials; expertise in gene editing techniques, including CRISPR
Work EnvironmentLaboratories focused on genetic modification, biotech companies, research institutionsResearch labs, biotech firms, academic settings
Industry UsagePrimarily in biotech, pharmaceuticals, agriculture, and researchSimilar industries, often overlapping in research projects

Both roles involve genetic modification techniques, with a focus on CRISPR technology. A Crispr Scientist specializes specifically in CRISPR-based methods, while a Gene Editing Researcher may work with various gene editing tools, including but not limited to CRISPR. The roles often overlap in credentials and work environment, but the Crispr Scientist emphasizes expertise in CRISPR technology.

More about Crispr Scientist jobs
What cities are hiring for Crispr Scientist jobs? Cities with the most Crispr Scientist job openings:
What states have the most Crispr Scientist jobs? States with the most job openings for Crispr Scientist jobs include:
What job categories do people searching Crispr Scientist jobs look for? The top searched job categories for Crispr Scientist jobs are:
Crispr Scientist jobs near you
Infographic showing various Crispr Scientist job openings in the United States as of July 2026, with employment types broken down into 5% Internship, 22% As Needed, 52% Full Time, 17% Part Time, 1% Contract, and 3% Nights. Highlights an 73% Physical, 1% Hybrid, and 26% Remote job distribution, with an average salary of $130,117 per year, or $62.6 per hour.
Senior Specialist, Drug Safety

Senior Specialist, Drug Safety

Crispr Therapeutics

Boston, MA

$105K - $115K/yr

Full-time

Re-posted 25 days ago

Job description

Job Description:

Company Overview

Founded over a decade ago,CRISPR Therapeuticsis a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY(exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia.CRISPR Therapeuticsis advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact,CRISPR Therapeuticshas established strategic collaborations with leading biopharmaceutical partners, includingVertex Pharmaceuticals.CRISPR Therapeutics AGis headquartered inZug,Switzerland, with its wholly-ownedU.S.subsidiary,CRISPR Therapeutics, Inc., and R&D operations based inBoston, MassachusettsandSan Francisco,California.

Position Summary

Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases. The successful candidate will work independently, playing a critical role in PV Case management to improve case quality, reconcile safety data and diving into ICSR processing activities.

Responsibilities

  • Data entry of ISCRs for select CRISPR programs
  • Quality Control of ICSRs for select CRISPR programs
  • Ensure timely submission and compliance of assigned ICSRs to global regulatory authorities, business partners, CROs and other parties.
  • Reconcile safety data with third parties.
  • Work closely with PV leadership to ensure PV compliance and inspection readiness.
  • Develop and maintain data entry guidelines and safety reporting forms
  • Develop and maintain training materials for data entry of ICSRs
  • Monitoring of ICSRs in workflow and managing processing timelines
  • As needed, support data readiness for generation and submission of aggregate reports (e.g., DSUR, PBRER, and IDMC listings).
  • Collaborate with functional leaders and stakeholders to recommend practical, high-impact solutions for PV case processing activities
  • Support ongoing PV initiatives and projects assigned by PV Leadership

Minimum Qualifications

  • Bachelor's degree in nursing, pharmacy, or other life sciences field
  • Minimum 5 years of experience in managing end-to-end ICSR case processing activities either at a Sponsor company or through PV vendor(s)
  • Knowledge of FDA, ICH, EU regulations and requirements
  • Meticulous attention to detail
  • Proficiency in MedDRA and WHO Drug dictionaries.
  • Experience with Veeva safety database, EDC systems.
  • Strong ability to prioritize and remain organized within a dynamic and ever-changing environment
  • Excellent verbal and written communication skills, strong attention to detail, and prior experience working cross-functionally.

Preferred Qualifications

  • Oncology and/or Cell & Gene Therapy experience preferred
  • Advanced degree in life sciences, nursing, pharmacy, or related healthcare profession.
  • Prior experience working on a nimble Pharmacovigilance Team in Biotech or small/medium size pharmaceutical company.

Competencies

  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.

CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.

Senior Specialist: Base pay range of $105,000 to $115,000+ bonus, equity and benefits

The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

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