Medical Writing Manager Jobs in Massachusetts
Medical Writing Manager jobs in Massachusetts are concentrated in the Greater Boston corridor, the Waltham-Lexington biotech belt, and the Cambridge life sciences cluster, where demand reaches from senior regulatory writers to directors overseeing global submission teams. Employers with a consistent Massachusetts presence include Pfizer, Biogen, and AstraZeneca, all of which maintain substantial medical affairs and regulatory writing functions in the state. Oncology, rare disease, and biologics documentation are among the most in-demand specialties for the role. See the openings below and apply to the ones that match your experience.
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Alexion- AstraZeneca Rare Disease is seeking a Medical Writing Intern to support the Medical Writing organization at its Boston-Seaport, Massachusetts location. The intern will contribute to clinical-regulatory documents, interpret complex scientific data, and support AI-based Medical Writing initiatives that improve content development and workflow efficiency.
Key Responsibilities- Co-author clinical-regulatory documents within a program, ensuring relevant regulatory, technical, and quality standards are achieved.
- Apply relevant processes and best practices to the development of clinical-regulatory documents.
- Contribute to AI-based Medical Writing initiatives that facilitate the automation of content or tasks for process improvement.
- Interpret complex clinical data and information and condense it into clear, concise, and accurate messages that address information requirements.
- Currently pursuing a PhD or a non-MBA Master’s Degree in Public Health, Pharmaceutical Science, Regulatory Science, Biological Science.
- Meeting the applicable graduation timeline requirements with an anticipated graduation date set for after August 2027.
- US Work Authorization is required at time of application. Applicants must have work authorization that does not require future sponsorship.
- This role will not be granting OPT support.
- Advanced proficiency with Microsoft Word functions.
- Strong writing and editing ability, including the ability to summarize data.
- Experience with electronic document management systems is a plus.
- Experience with AI-assisted drafting and summarization tools is a plus.
- Scientific or technical understanding.
- Critical-thinking and analytical skills.
- Strong communication and presentation skills.
- Ability to report on site to Boston-Seaport, MA 3 days a week. This role will not provide relocation assistance.
- Hourly range: $41- $48 (PhD)
- #earlytalent
Date Posted
23-Oct-2026Closing Date
19-Nov-2026Our 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.
Alexion- AstraZeneca Rare Disease is seeking a Medical Writing Intern to support the Medical Writing organization at its Boston-Seaport, Massachusetts location. The intern will contribute to clinical-regulatory documents, interpret complex scientific data, and support AI-based Medical Writing initiatives that improve content development and workflow efficiency.
Key Responsibilities- Co-author clinical-regulatory documents within a program, ensuring relevant regulatory, technical, and quality standards are achieved.
- Apply relevant processes and best practices to the development of clinical-regulatory documents.
- Contribute to AI-based Medical Writing initiatives that facilitate the automation of content or tasks for process improvement.
- Interpret complex clinical data and information and condense it into clear, concise, and accurate messages that address information requirements.
- Currently pursuing a PhD or a non-MBA Master’s Degree in Public Health, Pharmaceutical Science, Regulatory Science, Biological Science.
- Meeting the applicable graduation timeline requirements with an anticipated graduation date set for after August 2027.
- US Work Authorization is required at time of application. Applicants must have work authorization that does not require future sponsorship.
- This role will not be granting OPT support.
- Advanced proficiency with Microsoft Word functions.
- Strong writing and editing ability, including the ability to summarize data.
- Experience with electronic document management systems is a plus.
- Experience with AI-assisted drafting and summarization tools is a plus.
- Scientific or technical understanding.
- Critical-thinking and analytical skills.
- Strong communication and presentation skills.
- Ability to report on site to Boston-Seaport, MA 3 days a week. This role will not provide relocation assistance.
- Hourly range: $41- $48 (PhD)
- #earlytalent
Date Posted
23-Oct-2026Closing Date
19-Nov-2026Our 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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Where Massachusetts roles are concentrated, by current openings.
Medical Writing Manager Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
What Massachusetts Employers Look For
The qualifications that appear most often in medical writing manager jobs across Massachusetts.
- Bachelor's or advanced degree in life sciences, pharmacy, or a related scientific discipline
- Five or more years of regulatory or medical writing experience in a pharmaceutical or biotech setting
- Demonstrated experience managing or mentoring a team of medical writers
- Proficiency with CTD and eCTD submission formats for FDA regulatory filings
- Strong working knowledge of ICH guidelines and GCP documentation standards
- Experience writing clinical study reports, IND sections, or NDA submission documents
Medical Writing Manager Jobs in Massachusetts: Frequently Asked Questions
How do you become a medical writing manager in Massachusetts?
The most direct path is building several years of regulatory or clinical medical writing experience at a Massachusetts biotech or pharmaceutical employer before moving into a management role. No state-issued license is required for medical writing managers in Massachusetts. Many hiring managers in the state favor candidates who hold or pursue the American Medical Writers Association credential, which demonstrates professional writing and documentation standards relevant to FDA-regulated environments.
Which companies hire medical writing managers in Massachusetts?
Companies currently hiring medical writing managers in Massachusetts include AstraZeneca, AVEO Oncology, and Alkermes, per current listings on Migrate Mate as of October 2026. Massachusetts's dense concentration of life sciences headquarters and clinical research organizations means openings appear year-round across both large pharma and emerging biotech firms.
Which Massachusetts cities have the most medical writing manager jobs?
Boston, Cambridge, and Waltham account for the largest share of medical writing manager openings in Massachusetts. Greater Boston and Cambridge anchor the market because of their concentration of pharmaceutical headquarters, academic medical centers, and contract research organizations, while suburban hubs like Waltham and Lexington draw significant volume from the biotech corridor along Route 128.
Are there remote medical writing manager jobs in Massachusetts?
Yes, and more than most fields. Medical writing is inherently document-based, making it well suited to remote and hybrid arrangements. About 100% of medical writing manager openings tied to Massachusetts are remote or hybrid as of October 2026, reflecting how broadly the industry has embraced flexible work for writing and regulatory roles. Submission management and team oversight tasks are the functions most commonly performed remotely.
How can I get hired as a medical writing manager in Massachusetts with little or no experience?
The most realistic entry point is a staff or associate medical writer role at a Massachusetts biotech or contract research organization, then building toward management over several years. Large Massachusetts employers such as Biogen and Pfizer, along with contract research organizations based in the Boston area, regularly hire associate writers from clinical, pharmacy, or scientific communications backgrounds. A portfolio of regulatory documents and familiarity with FDA submission formats strengthens any application at the entry level.
Where can I find and apply to medical writing manager jobs in Massachusetts?
You can find and apply to medical writing manager jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings for the role. Search the listings to find positions that match your experience level and preferred location, then apply directly to the ones that fit.
See All 11 Medical Writing Manager Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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