The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary We are seeking a highly motivated Research Associate II to support the design ...
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary We are seeking a highly motivated Research Associate II to support the design ...
Associate Director / Director, Toxicology
Cambridge, MA · On-site
$185K - $260K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The Associate Director / Director, Toxicology will be responsible for the nonclinical safety ...
Associate Director / Director, Toxicology
Cambridge, MA · On-site
$185K - $260K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The Associate Director / Director, Toxicology will be responsible for the nonclinical safety ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The Associate Director serves as the enterprise owner of treatment center onboarding and quality ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The Associate Director serves as the enterprise owner of treatment center onboarding and quality ...
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary The Associate Director, Medical Safety is responsible for medical and clinical ...
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary The Associate Director, Medical Safety is responsible for medical and clinical ...
The Company continues to expand its leadership in gene editing through the development of ... Position Summary The Associate Director, Medical Safety is responsible for medical and clinical ...
The Company continues to expand its leadership in gene editing through the development of ... Position Summary The Associate Director, Medical Safety is responsible for medical and clinical ...
Senior / Principal Research Associate, In Vivo Studies
Cambridge, MA · On-site
$90K - $120K/yr
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
Quick apply
Senior / Principal Research Associate, In Vivo Studies
Cambridge, MA · On-site
$90K - $120K/yr
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
Senior / Principal Research Associate, In Vivo Studies
Cambridge, MA · On-site
$90K - $120K/yr
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
Senior / Principal Research Associate, In Vivo Studies
Cambridge, MA · On-site
$90K - $120K/yr
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
... gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research ... Associate to support the planning, execution, and analysis of in vivo pharmacology and ...
Associate in Systems Biology
Cambridge, MA · On-site
$60K - $70K/yr
Position Details Title Associate in Systems Biology School Harvard Medical School Department/Area ... gene-editing approaches, and the application of molecular techniques to fundamental biological ...
Associate in Systems Biology
Cambridge, MA · On-site
$60K - $70K/yr
Position Details Title Associate in Systems Biology School Harvard Medical School Department/Area ... gene-editing approaches, and the application of molecular techniques to fundamental biological ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts Quality ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts Quality ...
Associate Manager, CMC Operations
South Boston, MA · On-site
$110K - $120K/yr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary The Associate Manager, CMC Operations supports the CMC Lead across multiple ...
Associate Manager, CMC Operations
South Boston, MA · On-site
$110K - $120K/yr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary The Associate Manager, CMC Operations supports the CMC Lead across multiple ...
Associate Manager, CMC Operations
Boston, MA · On-site
$110K - $120K/yr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary The Associate Manager, CMC Operations supports the CMC Lead across multiple ...
Associate Manager, CMC Operations
Boston, MA · On-site
$110K - $120K/yr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary The Associate Manager, CMC Operations supports the CMC Lead across multiple ...
Senior Manager/Associate Director, Biostatistics
Cambridge, MA · On-site
$155K - $225K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... Beam is seeking a Senior Manager/Associate Director, Biostatistics to support the statistical ...
Senior Manager/Associate Director, Biostatistics
Cambridge, MA · On-site
$155K - $225K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... Beam is seeking a Senior Manager/Associate Director, Biostatistics to support the statistical ...
Clinical Trial Associate
Boston, MA · On-site
$36.50 - $49.75/hr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary Working closely with the Clinical Trial Manager, the Clinical Trial Associate (CTA ...
Clinical Trial Associate
Boston, MA · On-site
$36.50 - $49.75/hr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary Working closely with the Clinical Trial Manager, the Clinical Trial Associate (CTA ...
Clinical Trial Associate
South Boston, MA · On-site
$36.50 - $49.75/hr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary Working closely with the Clinical Trial Manager, the Clinical Trial Associate (CTA ...
Clinical Trial Associate
South Boston, MA · On-site
$36.50 - $49.75/hr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary Working closely with the Clinical Trial Manager, the Clinical Trial Associate (CTA ...
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Associate Director: * 12+ Years of relevant experience with a bachelor's degree * 10+ Years of ...
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Associate Director: * 12+ Years of relevant experience with a bachelor's degree * 10+ Years of ...
We are seeking a Public Relations Associate to support the development and execution of ... editing, and communication skills Ability to manage multiple tasks with precision and ...
We are seeking a Public Relations Associate to support the development and execution of ... editing, and communication skills Ability to manage multiple tasks with precision and ...
Associate Director, Clinical Scientist
South Boston, MA · On-site
$170K - $185K/yr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary CRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to ...
Associate Director, Clinical Scientist
South Boston, MA · On-site
$170K - $185K/yr
The Company continues to expand its leadership in gene editing through the development of ... Position Summary CRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to ...
Associate Director, Clinical Scientist
Boston, MA · On-site
$170K - $185K/yr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary CRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to ...
Associate Director, Clinical Scientist
Boston, MA · On-site
$170K - $185K/yr
The Company continues to expand its leadership in gene editing through the development of SyNTase ... Position Summary CRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to ...
## Associate Director, Clinical ScientistApplyremote type: Site Basedlocations: South Boston, MAtime ... The Company continues to expand its leadership in gene editing through the development of SyNTaseTM ...
## Associate Director, Clinical ScientistApplyremote type: Site Basedlocations: South Boston, MAtime ... The Company continues to expand its leadership in gene editing through the development of SyNTaseTM ...
Associate Editor information
See Quincy, MA salary details
$14.91 - $18.18
5% of jobs
$18.18 - $21.44
10% of jobs
$22.61 is the 25th percentile. Wages below this are outliers.
$21.44 - $24.70
27% of jobs
The median wage is $26.22 / hr.
$24.70 - $27.96
16% of jobs
$30.84 is the 75th percentile. Wages above this are outliers.
$27.96 - $31.23
18% of jobs
$31.23 - $34.49
12% of jobs
$34.49 - $37.75
8% of jobs
$37.75 - $41.01
2% of jobs
$41.01 - $44.28
0% of jobs
$44.28 - $47.54
0% of jobs
$47.54 - $50.80
1% of jobs
$14
$28
$50
How much do associate editor jobs pay per hour?
What does an associate editor do?
What are the key skills and qualifications needed to thrive as an associate editor?
What are some common challenges an associate editor might face when balancing multiple projects and deadlines?
What is the difference between Associate Editor vs Copy Editor?
| Aspect | Associate Editor | Copy Editor |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in editing or publishing | Bachelor's degree, strong language and grammar skills |
| Work Environment | Editorial teams in publishing, media, or academic settings | Publishing houses, magazines, online media |
| Employer & Industry Usage | Used in publishing, journalism, academic publishing | Common in editing, publishing, media industries |
| Primary Focus | Content acquisition, editorial decision-making, overseeing projects | Grammar, style, clarity, and correctness of text |
While both roles are vital in publishing, an Associate Editor typically handles content selection and editorial oversight, whereas a Copy Editor focuses on refining language, grammar, and style. The Associate Editor often manages multiple projects and collaborates with writers, while the Copy Editor ensures the final text is polished and error-free.
What are the most commonly searched types of Editor jobs in Quincy, MA?
The most popular types of Editor jobs in Quincy, MA are:
What are popular job titles related to Associate Editor jobs in Quincy, MA?
For Associate Editor jobs in Quincy, MA, the most frequently searched job titles are:
What job categories do people searching Associate Editor jobs in Quincy, MA look for?
The top searched job categories for Associate Editor jobs in Quincy, MA are:
What cities near Quincy, MA are hiring for Associate Editor jobs?
Cities near Quincy, MA with the most Associate Editor job openings:

Full-time
Re-posted 11 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
We are seeking a highly motivated Research Associate II to support the design, development, and optimization of novel lipid nanoparticle (LNP) formulations to advance our non-viral delivery platform for hepatic and extra-hepatic tissues, and enable next-generation genome editing therapies from discovery through clinical translation.
The ideal candidate will bring hands-on expertise in LNP formulation development, scale-up, analytical characterization, chemistry, and process development, with a strong passion for innovation in nucleic acid delivery technologies. This individual will join the dynamic, fast-growing, and highly collaborative CRISPR-X division and contribute to both platform technology innovation and preclinical therapeutic programs.
In this role, the candidate will work cross-functionally to develop and characterize advanced delivery systems for emerging editing modalities, helping drive transformative gene editing therapies toward patients with unmet medical needs.
Responsibilities
- Design, optimize, characterize, and execute lipid nanoparticle (LNP) formulations across a diverse range of lipid compositions and therapeutic payloads with minimal supervision.
- Apply hands-on expertise in LNP analytical characterization techniques, including RiboGreen assays, DLS, NanoFCM, NTA, TFF, endotoxin testing, and HPLC, as well as molecular biology methods such as DNA/RNA extraction, ELISA, SDS-PAGE, PCR, and Western blotting.
- Generate high-quality, reproducible datasets and maintain accurate, detailed experimental documentation in electronic laboratory notebooks (ELNs).
- Perform mammalian cell culture and support in vitro studies, including transient transfection and electroporation in established cell lines. Collaborate cross-functionally with process development, analytical, and in vivo teams to support reproducible manufacturing processes and advance programs toward clinical development.
- Contribute to platform innovation by investigating LNP mechanisms of action to improve delivery efficiency, therapeutic potency, and formulation stability.
- Present experimental results, technical findings, and project updates to cross-functional teams and broader organizational audiences.
- Effectively manage multiple priorities and projects in a fast-paced, highly collaborative research environment.
Minimum Qualifications
- BS or MS in Chemistry, Chemical Engineering, Biochemistry, or a related scientific discipline.
- Relevant industry or academic research experience:
- Research Associate II: 2-5+ years with a bachelor's degree or 0-2+ years of relevant experience with a master's degree
- Hands-on experience in lipid nanoparticle (LNP) formulation and analytical characterization for nucleic acid and targeted delivery applications.
- Strong understanding of drug delivery systems and gene editing therapeutics.
- Demonstrated ability to work independently while contributing effectively within a fast-paced, results-driven, and collaborative research environment.
- Highly organized with strong scientific rigor, problem-solving skills, and attention to detail.
Preferred Qualifications
- Experience with high-throughput formulation screening and knowledge of microfluidic mixing process.
- Prior experience of ionizable lipid design, bioconjugation, and process development preferred.
- Prior experience with scale-up and large-scale manufacturability development of LNPs.
- Understanding of RNA engineering, molecular biology, and hands-on experience of maintaining cells and performing in vitro transfection.
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.
Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site.
Research Associate II: Base pay range of $85,000 to $92,000 + discretionary 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
About CRISPR Therapeutics
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
Boston, MA, US
Year founded
2013