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Crispr Therapeutics Jobs (NOW HIRING)

Crispr Therapeutics

Clinical Trial Associate

Boston, MA

$36.50 - $49.75/hr

CRISPR Therapeutics AGis headquartered inZug,Switzerland, with its wholly-ownedU.S.subsidiary,CRISPR Therapeutics, Inc., and R&D operations based inBoston, MassachusettsandSan Francisco,California.

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How much do crispr therapeutics jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for crispr therapeutics in the United States is $31.48, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $40.14 per hour, depending on experience, location, and employer.

What is a Crispr Therapeutics?

A CRISPR Therapeutics job typically involves working with gene-editing technologies to develop treatments for genetic diseases. Employees may work in research, development, clinical trials, or regulatory roles to advance CRISPR-based therapies. Positions range from scientists and bioengineers to project managers and regulatory specialists. The goal is to translate CRISPR technology into real-world medical applications.

What does a Crispr Therapeutics do?

In a CRISPR Therapeutics role, your day-to-day tasks often include designing and conducting experiments, analyzing genomic data, and troubleshooting laboratory protocols related to gene editing projects. You’ll work closely with scientists across functional teams, such as protein engineers, bioinformaticians, and clinical researchers, to advance therapeutic candidates from discovery through preclinical stages. Regular meetings to discuss results and plan next steps are common, and documentation of experiments and findings is crucial for regulatory compliance. Staying up to date with the latest scientific literature and adapting to new techniques is also an ongoing part of the job.

What are the key skills and qualifications needed to thrive in a Crispr Therapeutics position?

To excel in CRISPR Therapeutics roles, candidates typically need a solid background in molecular biology, genetics, or biotechnology, along with a relevant advanced degree (e.g., Ph.D., M.Sc., or B.Sc. with experience). Familiarity with genome editing technologies such as CRISPR-Cas9, cell culture systems, PCR, and next-generation sequencing is crucial, and certifications in laboratory safety or bioinformatics can be valuable. Strong analytical thinking, problem-solving, attention to detail, and the ability to collaborate within multidisciplinary research teams set top performers apart. These skills and qualities are vital for ensuring rigorous scientific research, innovation, and effective teamwork in a rapidly evolving biotech environment.

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Crispr Therapeutics jobs near you
Infographic showing various Crispr Therapeutics job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 93% Full Time, 3% Part Time, and 2% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $65,473 per year, or $31.5 per hour.

Statistical Programming Contractor (16-Month Contract)

Crispr Therapeutics

Boston, MA • On-site

$70 - $80/hr

Full-time

Posted 16 days ago

Job description

Job Description:

Company Overview

ounded 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

The Statistical Programming Contractor will provide technical support for statistical programming activities for assigned clinical studies, FDA submissions, and the development of initiatives.

Responsibilities

  • Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data.
  • Have thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets
  • Program edit checks and produce quality tables, figures and listings in a timely fashion and high quality.
  • Work closely with Clinical Operations, Data Management and Biostatisticians on various clinical projects so that data analysis can be performed in a timely fashion.

Minimum Qualifications

  • Bachelor's Degree in Statistics, Mathematics, and/or Computer Science/IT background. Master's Degree preferred.
  • Minimum 3years of statistical programming in a pharmaceutical/biotech or CRO setting (depending on level)
  • Strong knowledge in CDISC including SDTM, ADaM, metadata, controlled terminologies, and data flows, as well as in industry standards for electronic submission of data to FDA.
  • Strong hands-on SAS programing skills and working experience for clinical trial reporting for SDTM, ADaM, Table, figure, and Listing.
  • Excellent working knowledge of SAS/BASE, SAS/STAT, SAS/GRAPH and SAS Macro language.
  • Advanced knowledge of GCP/ICH standards, 21 CFR Part 11.

Preferred Qualifications

  • Strong ability to work within cross-functional teams.
  • Excellent interpersonal, organizational, and multi-tasking skills.

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.

Base pay range of $70.00 - $80.00 per hour.

The hourly rate provided is the reasonable estimate for this contract position. 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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