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Writing Associate Jobs in Everett, MA (NOW HIRING)

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 ...

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 ...

The Associate Director, Medical Writing Science manages the overall operations of a team or major project and implements this through effective leadership. This role provides guidance and leadership ...

Warehouse Associate

Braintree, MA · On-site

$17 - $20.25/hr

Homans Associates is a subsidiary of the largest independent HVAC/R distribution company in the ... Excellent communication (written and oral) and interpersonal (Teambuilding) skills * Proven ...

Associate

Boston, MA · On-site

$80K - $100K/yr

Associates are talent recruiters, relationship builders, writers, and project managers. They support the project work of Partners who build client relationships, develop business, and ensure the ...

Associate

Boston, MA

$80K - $100K/yr

Associates are talent recruiters, relationship builders, writers, and project managers. They support the project work of Partners who build client relationships, develop business, and ensure the ...

Associate

Boston, MA · On-site +1

$80K - $100K/yr

Associates are talent recruiters, relationship builders, writers, and project managers. They support the project work of Partners who build client relationships, develop business, and ensure the ...

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Writing Associate information

See Everett, MA salary details

$47.4K

$111.4K

$177.6K

How much do writing associate jobs pay per year?

As of May 28, 2026, the average yearly pay for writing associate in Everett, MA is $111,364.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,400.00 and $133,900.00 per year, depending on experience, location, and employer.

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.

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 Writing Associates?

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 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 are the most commonly searched types of Writing jobs in Everett, MA? The most popular types of Writing jobs in Everett, MA are:
What are popular job titles related to Writing Associate jobs in Everett, MA? For Writing Associate jobs in Everett, MA, the most frequently searched job titles are:
What job categories do people searching Writing Associate jobs in Everett, MA look for? The top searched job categories for Writing Associate jobs in Everett, MA are:
What cities near Everett, MA are hiring for Writing Associate jobs? Cities near Everett, MA with the most Writing Associate job openings:
Clinical Regulatory Writer (Associate Director or Manager)

Clinical Regulatory Writer (Associate Director or Manager)

AstraZeneca

Boston, MA • On-site

$169.94K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 70 rated pharmaceutical


Job description

Job Title: Clinical Regulatory Writer, Associate Director or Manager
Location: Boston, MA - Hybrid (3 days onsite)
Introduction to role:
Are you ready to be part of the solution, turning drug development strategies into reality? As a Clinical Regulatory Writer, you will play a pivotal role in translating life-changing science into medicines. Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We support AstraZeneca's core therapeutic areas across all phases of clinical development, striving for excellence in communication to achieve successful submissions and approvals.
Accountabilities:
As a Clinical Regulatory Writer, you will:
  • Independently manage clinical regulatory writing activities across a complex portfolio of work.
  • Author the most complex clinical-regulatory documents within a program, ensuring regulatory, technical, and quality standards are met.
  • Provide strategic communications leadership to projects, establishing communication standards and advocating for quality and efficiency.
  • Drive the development of the clinical Submission Communication Strategy (cSCS) when acting as a submission lead.
  • Lead internal/external authoring teams and partner with vendor medical writers to ensure timely and quality delivery.
  • Interpret complex data and information, condensing it into clear, concise messages that meet customer information requirements.
  • Demonstrate strategic thinking and review capabilities.
  • Collaborate proactively with other functions at the program level.
  • Support the development of Clinical Regulatory Writing Managers.
  • Drive continuous improvement and operational excellence from a communications leadership perspective.
    Essential Skills/Experience:
  • Education/Experience required:
    Associate Director level : BS Life Sciences degree or simiilar, 7+ yrs medical writing experience in pharmaceutical industry or CRO.
  • Manager level: BS Life Sciences degree or simiilar, 2-7+ yrs medical writing experience in pharmaceutical industry or CRO
  • Ability to advise and lead communication projects.
  • Understand drug development and communication process from development, launch through life cycle management.
  • In-depth knowledge of the technical and regulatory requirements related to the role.

Desirable Skills/Experience:
  • Advanced degree in a scientific discipline (Ph.D.)
  • Experience with CSR, CTD module 2 summaries
  • Experience leading clinical submission (NDA/BLA/MAA)
  • Experience developing clinical submission communication strategy

This is a Hybrid role - minimum requirment 3 days per week onsite
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
AstraZeneca is where innovation meets collaboration. We harness diverse knowledge to move with agility, working seamlessly across functions globally. Our team is empowered to make quick decisions, influencing drug development strategy at all levels. With a science-driven approach, we bring life-changing medicines to patients, constantly asking questions and trying new things. Your professional growth is passionately supported here, with opportunities to work on projects at all stages of development.
Ready to make an impact? Apply now and be part of our dynamic team!
The annual base pay (or hourly rate of compensation) for this position ranges from $133,042.40 - $199,563.60 USD Annual for Associate Director level, and $ 113,293.60 - $169,940.40 USD Annual for Manager level. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
13-May-2026
Closing Date
31-May-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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