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Writing Associate Jobs in Holden, MA (NOW HIRING)

Alkermes

Associate Director, Medical Writing

Waltham, MA · Hybrid

$175K - $190K/yr

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on ...

Alkermes

Associate Director, Medical Writing

Waltham, MA · On-site

$175K - $190K/yr

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on ...

PetSmart

PetsHotel Associate

Framingham, MA · On-site

Effective written and verbal communication skills. PHYSICAL DEMANDS AND WORK ENVIRONMENT * Associate required to stand, walk, climb a ladder, and use hands to handle, feel, hold, write, etc. The ...

O'Hagan Meyer

Associate Attorney

Needham, MA · On-site

$125K - $150K/yr

O'Hagan Meyer is seeking an Associate Attorney with 4-6 years of litigation experience to join our ... Candidates should demonstrate outstanding writing, research, and analytical skills, as well as ...

O'Hagan Meyer

Associate Attorney

Needham, MA

$125K - $150K/yr

O'Hagan Meyer is seeking an Associate Attorney with 4-6 years of litigation experience to join our ... Candidates should demonstrate outstanding writing, research, and analytical skills, as well as ...

O'Hagan Meyer

Associate Attorney

Needham, MA · On-site

$125K - $150K/yr

O'Hagan Meyer is seeking an Associate Attorney with 4-6 years of litigation experience to join our ... Candidates should demonstrate outstanding writing, research, and analytical skills, as well as ...

Topkins & Bevans

Attorney Associate

Waltham, MA · On-site

$65K - $75K/yr

We are seeking an Attorney Associate to become a part of our team! You will represent clients in ... Excellent written and verbal communication skills * Must be a Massachusetts Notary Public Company ...

Manufacturing Company

Warehouse Associate

Northborough, MA · On-site

$16.50 - $19.50/hr

About the job Warehouse Associate We are seeking a highly physical and dependable Warehouse ... Reading and writing English to process orders, read labels, and manage incoming and outgoing ...

Brandeis University

Research Associate I

Waltham, MA · On-site

The Research Associate contributes to all phases and aspects of research projects as a member of ... Primary responsibilities include grant writing, research design, data collection and analysis, and ...

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All JobsWriting Associate JobsWriting Associate Jobs in Holden, MA

Writing Associate information

See Holden, MA salary details

$49.1K

$115.5K

$184.1K

How much do writing associate jobs pay per year?

As of Aug 3, 2026, the average yearly pay for writing associate in Holden, MA is $115,458.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,400.00 and $138,800.00 per year, depending on experience, location, and employer.

How does a writing associate typically collaborate with other team members during the content development process?

A Writing Associate often works closely with editors, subject matter experts, and designers to ensure content accuracy, clarity, and alignment with project goals. Collaboration may involve participating in brainstorming sessions, revising drafts based on feedback, and adapting writing styles to suit various platforms. Regular communication and feedback loops are essential, as Writing Associates need to balance creative input with organizational guidelines and deadlines. This teamwork not only enhances content quality but also provides opportunities to learn from experienced colleagues.

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

To thrive as a Writing Associate, you need strong writing, editing, and research skills, typically supported by a bachelor's degree in English, communications, or a related field. Familiarity with style guides (such as APA or MLA), word processing software, and collaborative platforms like Google Docs is often required. Exceptional communication, critical thinking, and adaptability help you tailor content and feedback to diverse audiences. These competencies are crucial for producing clear, effective writing and supporting the development of others’ written work.

What is the difference between Writing Associate vs Writing Tutor?

AspectWriting AssociateWriting Tutor
CredentialsTypically requires a bachelor's degree, strong writing skillsUsually undergraduate or graduate students with good writing abilities
Work EnvironmentOften works in academic or professional settings, supporting writing projectsPrimarily works in tutoring centers or academic support services
Employer & IndustryUniversities, colleges, or writing centersEducational institutions, tutoring centers

While both roles involve supporting writing, a Writing Associate often collaborates on projects and may have more responsibilities related to content development, whereas a Writing Tutor primarily provides one-on-one assistance to students to improve their writing skills.

What is a writing associate?

Writing Associates are professionals who assist students, faculty, or professionals with writing projects. They provide feedback, guidance, and support to help individuals improve the clarity, structure, and effectiveness of their written work. Writing Associates often work in academic settings, such as writing centers or universities, but can also be found in corporate or nonprofit environments. Their goal is to empower writers to develop their skills and produce high-quality documents.
What cities near Holden, MA are hiring for Writing Associate jobs? Cities near Holden, MA with the most Writing Associate job openings:
Writing Associate jobs near you

Associate Director, Medical Writing

Alkermes

Waltham, MA • Hybrid

$175K - $190K/yr

Full-time

Re-posted 20 days ago

Job description

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on writing expertise with responsibilities for resource planning and matrix leadership to deliver high-quality, fit-for-purpose clinical and regulatory documents aligned with program and regulatory objectives. The Associate Director is accountable for document development strategy, planning, and execution; leads clinical content development for complex submissions (including content strategy, organization, and resourcing); and partners with Clinical Development, Regulatory Affairs, Biostatistics, and other key functions to ensure cohesive messaging, mitigate risk, and support successful regulatory interactions and filings. The Associate Director applies advanced technical judgment to solve complex problems and ensures Medical Writing activities are integrated with broader development and regulatory objectives.

Why join Team Alkermes?

Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. 

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law.  Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Alkermes is an E-Verify employer.

  • Advanced degree (PhD, PharmD, or equivalent) in a relevant discipline.

  • 8+ years of relevant experience in medical writing, clinical research, or a related function.

  • Experience supporting marketing authorization applications (NDA/BLA/MAA), IND submissions, and other major regulatory filings.
  • Demonstrated ability to lead complex projects, plan and optimize resources (internal staff, vendors, and tools), and manage competing priorities.

  • Strong ability to work independently, navigate ambiguity, and resolve complex, non-routine problems through pragmatic risk mitigation.

  • Broad scientific understanding across multiple therapeutic areas; neuroscience experience preferred but not required.

  • Excellent written and verbal communication skills, with proven ability to influence and collaborate across diverse teams.

Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work. 

The annual base salary for this position ranges from $175,000 - $190,000. In addition, this position is eligible for an annual performance pay bonus.  Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package.  Additional details can be found on our careers website: www.alkermes.com/careers#working-here  

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  • Accountable for medical writing deliverables across one or more clinical programs, contributing to program-level plans and ensuring aligned timelines, quality, and resourcing.

  • Independently author and lead the planning, review, comment resolution, and delivery of routine and complex clinical and regulatory documents.

  • Lead or coordinate clinical content development for complex regulatory submissions, ensuring messaging alignment with regulatory strategy and development objectives.

  • Serve as the primary medical writing lead on program teams, proactively identifying risks, anticipating cross-functional challenges, and driving issue resolution.

  • Oversee outsourced writing support, setting expectations, managing review cycles, and ensuring inspection-ready quality.

  • Contribute to the development and execution of Medical Writing departmental goals, including process improvements, inspection readiness initiatives, and adoption of new tools and technologies.

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