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Associate Editor Jobs in Lexington, MA (NOW HIRING)

GLFHC

Marketing Associate

Methuen, MA

The Marketing Associate will play a pivotal role in executing marketing and communication plans ... Exceptional writing, editing, and verbal communication skills, including the ability to tailor ...

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All JobsAssociate Editor JobsAssociate Editor Jobs in Lexington, MA

Associate Editor information

See Lexington, MA salary details

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How much do associate editor jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for associate editor in Lexington, MA is $30.62, according to ZipRecruiter salary data. Most workers in this role earn between $24.57 and $34.28 per hour, depending on experience, location, and employer.

What are some common challenges an associate editor might face when balancing multiple projects and deadlines?

Associate Editors often juggle several articles or publications at once, each with its own timeline and set of contributors. A common challenge is prioritizing tasks effectively to meet tight deadlines while maintaining editorial quality and accuracy. This role requires strong organizational skills and clear communication with writers, senior editors, and other team members to ensure everyone is aligned. Developing efficient workflows and being adaptable to sudden changes—such as urgent revisions or shifting editorial calendars—are essential for success in this fast-paced environment.

What is the difference between Associate Editor vs Copy Editor?

AspectAssociate EditorCopy Editor
Required CredentialsBachelor's degree, experience in editing or publishingBachelor's degree, strong language and grammar skills
Work EnvironmentEditorial teams in publishing, media, or academic settingsPublishing houses, magazines, online media
Employer & Industry UsageUsed in publishing, journalism, academic publishingCommon in editing, publishing, media industries
Primary FocusContent acquisition, editorial decision-making, overseeing projectsGrammar, 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 does an associate editor do?

An Associate Editor is responsible for supporting the editorial process at a publication or media outlet. Their tasks usually include reviewing submissions, editing articles for clarity and accuracy, coordinating with writers and contributors, and helping manage deadlines. Associate Editors often assist in shaping content strategy and may contribute their own writing as well. They work closely with senior editors to ensure the quality and consistency of published materials.

What are the key skills and qualifications needed to thrive as an associate editor?

To excel as an Associate Editor, you need strong writing, editing, and research skills, often backed by a degree in English, journalism, or a related field. Familiarity with content management systems (CMS), style guides (like AP or Chicago), and editing software is typically required. Attention to detail, organization, and effective communication are crucial soft skills for managing deadlines and collaborating with writers. These abilities ensure content accuracy, quality, and timely publication in a fast-paced editorial environment.
What are the most commonly searched types of Editor jobs in Lexington, MA? The most popular types of Editor jobs in Lexington, MA are:
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Associate Editor jobs near you
Infographic showing various Associate Editor job openings in Lexington, MA as of August 2026, with employment types broken down into 2% Internship, 77% Full Time, 18% Part Time, and 3% Contract. Highlights an 77% In-person, 6% Hybrid, and 17% Remote job distribution, with an average salary of $63,692 per year, or $30.6 per hour.

Senior / Principal Research Associate, In Vivo Studies

Pivotal

Cambridge, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

Job description

Salary: Salary Range $90,000 - $120,000 per year

Senior / Principal Research Associate, In Vivo Studies

Location: Boston, MA

Reports to: Scientist II

Job Type: Full time, Onsite

About Us

We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo 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 biodistribution studies that advance our preclinical programs. This is a hands-on role for a scientifically rigorous, highly organized researcher who can execute rodent studies, collect high-quality samples, maintain strong study records, and partner closely with Translational Research, Delivery, Editing, and Program teams. The location for this position is expected to be onsite in our Boston lab.

Responsibilities

  • Support the design, planning, and execution of in vivo rodent studies evaluating delivery, biodistribution, editing efficiency, pharmacodynamic activity, tolerability, and related preclinical endpoints.
  • Perform hands-on in vivo study activities under approved protocols, which may include animal handling, dosing support, clinical observations, body weight tracking, sample collection, necropsy support, and tissue harvest.
  • Prepare study materials, dosing solutions, collection supplies, labels, chain-of-custody documentation, and sample inventories to ensure studies run smoothly and reproducibly.
  • Process blood, plasma, serum, bone marrow, spleen, liver, and other tissues for downstream molecular, cellular, and protein-based analyses, including nucleic acid and protein extraction workflows.
  • Coordinate with internal scientists and external partners or CROs to align study timelines, protocols, sample logistics, data transfers, and documentation requirements.
  • Maintain accurate electronic and paper study records, including protocols, worksheets, sample maps, deviations, reagent logs, and raw data consistent with data integrity and reproducibility expectations.
  • Analyze and summarize study observations and sample metadata; contribute to interpretation of in vivo results in the context of program goals.
  • Contribute to protocol development, study reports, SOPs, and continuous improvement of in vivo operations and sample-processing workflows.
  • Present study updates, operational risks, and key results in team meetings; collaborate cross-functionally with Translational Research, Delivery, Editing, and broader research teams.
  • Mentor or train junior team members on study preparation, sample handling, documentation practices, and relevant laboratory workflows as appropriate for level.

Qualifications

  • BS or MS in biology, pharmacology, molecular biology, biomedical sciences, veterinary technology, or a related discipline, with approximately 5-6 years of relevant hands-on research experience in industry or an equivalent research setting.
  • Direct experience supporting in vivo rodent studies, including study setup, animal handling, dosing support or study procedures, sample collection, tissue harvest, and post-collection processing.
  • Strong understanding of in vivo study execution, sample traceability, protocol adherence, and the importance of accurate, contemporaneous documentation.
  • Hands-on experience with downstream tissue and sample processing for molecular, cellular, or protein-based assays such as qPCR / RT-qPCR, ddPCR, ELISA, flow cytometry, Western blot / Jess, sequencing, or related analytical readouts.
  • Ability to plan daily study activities, anticipate operational needs, troubleshoot issues, and communicate risks or deviations promptly.
  • Comfort working in a fast-paced, cross-functional research environment with changing program priorities and multiple concurrent studies.
  • Clear written and verbal communication skills; comfortable summarizing study status, sample inventories, observations, and data for a scientific audience.
  • Commitment to high-quality animal care, ethical research practices, and compliance with approved study protocols, SOPs, and institutional requirements.

Preferred Qualifications

  • Experience supporting in vivo studies for gene editing, nucleic acid therapeutics, cell or gene therapy, biologics, or targeted delivery platforms.
  • Experience with LNP-based, antibody-based, receptor-targeted, or other delivery technologies in preclinical models.
  • Familiarity with biodistribution, pharmacodynamic, toxicology, or translational biomarker study designs.
  • Experience with common rodent dosing or sampling routes such as IV, IP, SC, PO, retro-orbital, submandibular, tail vein, or terminal cardiac collection, as applicable to approved protocols.
  • Experience processing hematopoietic tissues or working with bone marrow, spleen, peripheral blood, HSC / HSPC biology, immune-cell phenotyping, or flow cytometry workflows.
  • Experience coordinating external CRO studies, shipping biological samples, managing sample manifests, or reconciling datasets across internal and external teams.
  • Familiarity with electronic lab notebooks, study management systems, animal facility systems, or inventory / sample tracking tools.
  • Prior experience supporting IND-enabling, GLP-like, or regulated preclinical studies.

Benefits

  • Competitive salary, equity, and comprehensive benefits package.
  • Opportunities for professional growth and leadership development.
  • Fast-paced, collaborative, and innovative work environment.
  • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity.

How to Apply

Interested candidates will click Apply to proceed to our application portal and will need to submit a resume and cover letter detailing relevant experience. To be considered for the role, applicants must be:

  • Eligible to work in the United States for any employer without current or future sponsorship.
  • Able to work onsite in the lab, based on the location listed for the position (either San Diego, CA or Boston, MA). Please check the position listing when you Apply for the location of each role.
  • Direct candidates only and not from a third party, i.e., staffing agency.

Equal Opportunity Employer

We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

Salary Range

$90,000 - $120,000