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How much do crispr jobs pay per year?

As of Jul 11, 2026, the average yearly pay for crispr in the United States is $56,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $47,000.00 per year, depending on experience, location, and employer.

What types of projects or research might I work on as a CRISPR Scientist?

As a CRISPR Scientist, you may contribute to projects ranging from basic research in gene function and disease mechanisms to applied initiatives like crop improvement, gene therapy development, or pharmaceutical innovation. Your day-to-day responsibilities might include designing and executing gene-editing experiments, analyzing genetic data, collaborating with interdisciplinary teams, and documenting results for publication or regulatory submissions. Depending on your employer, you could work in academia, biotechnology, agriculture, or medical research industries. This role offers opportunities to make impactful scientific discoveries and gain exposure to emerging technologies, providing a strong foundation for career advancement within the field.

What are the key skills and qualifications needed to thrive in the Crispr position, and why are they important?

To thrive in a CRISPR Scientist role, you need a solid background in molecular biology, genetics, and gene-editing techniques, typically supported by an advanced degree in a life science discipline. Familiarity with laboratory equipment, gene-editing platforms like CRISPR-Cas9, and certifications in genetic engineering or molecular techniques are highly valuable. Attention to detail, critical thinking, and strong teamwork capabilities are key soft skills in this position. These skills are crucial to ensure safe, accurate, and innovative application of gene-editing technologies in research or therapeutics.

What is a CRISPR job?

A CRISPR job typically involves working with CRISPR-Cas9 or related gene-editing technologies in fields such as biomedical research, agriculture, or biotechnology. Professionals in this field may design, execute, and analyze gene-editing experiments to modify DNA for therapeutic, industrial, or scientific purposes. Roles can range from research scientists to bioinformatics specialists and lab technicians. Strong knowledge of molecular biology, genetics, and bioengineering is often required.

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Crispr jobs near you
Infographic showing various Crispr job openings in the United States as of July 2026, with employment types broken down into 74% Full Time, 25% Part Time, and 1% Contract. Highlights an 73% Physical, 1% Hybrid, and 26% Remote job distribution, with an average salary of $56,057 per year, or $27 per hour.
Senior Manager, Drug Safety

Senior Manager, Drug Safety

Crispr Therapeutics

South Boston, MA • On-site

$140K - $155K/yr

Full-time

Re-posted 21 days ago

Job description

Job Description:
Company Overview
Founded over a decade ago, CRISPR Therapeutics is 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 Therapeutics is 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 Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California.
Position Summary
Reporting to the Head of Pharmacovigilance Operations, the Senior Manager, Drug Safety will play a pivotal role in compliance oversight, end-to-end case management and author drug safety SOPs. The successful candidate will work cross-functionally to support Individual Case Safety Report (ICSR) processing and compliance and vendor management. This role will play part in ensuring continuity across all Pharmacovigilance activities.
Responsibilities
  • Oversee daily (ICSR) processing activities, escalating cases when necessary and perform quality checks to ensure compliance
  • Safety Database management and oversight (e.g. Study configuration, system updates and enhancements, MedDRA, WhoDRUG)
  • Collaborate with internal partners and external collaborators actively manage and safety data flow
  • Develop and implement Drug Safety SOPs and maintaining compliance to internal procedures
  • Participate in clinical study activities (start up, reconciliation and close out as assigned)
  • Train drug safety teams on established procedures and oversee compliance
  • Serve as the subject matter expert for ICSR intake processes and regulatory expectations, including presentations for Development Leadership
  • Lead aggregate safety reporting activities (DSUR)
  • Coordinate Safety Governance Scheduling
  • Create, track, monitor Key Performance Indicators (KPIs) and metrics for vendor performance monitoring and adherence to drug safety SOPs internally.
  • Ensure compliance oversight of Pharmacovigilance Agreements
  • Support audits and inspections as assigned.

Minimum Qualifications
  • Bachelor's degree in life sciences, nursing, pharmacy, or related healthcare profession with 10+ years of relevant experience.
  • Strong understanding of global pharmacovigilance regulations, ICSR processes, and the adverse event lifecycle.
  • Veeva Safety Database experience
  • Ability to independently identify, analyze, and solve complex operational and data-related issues.
  • Excellent written and verbal communication skills; able to convey complex concepts clearly.
  • Strong organizational, prioritization, and project-management capabilities.
  • Demonstrated ability to work collaboratively across functions and with external partners.
  • Strong attention to detail and commitment to data quality and compliance.

Preferred Qualifications
  • 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.
  • Cell and Gene Therapy / Oncology Experience

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 Manager, Drug Safety: Base pay range of $140,000 to $155,000+ 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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