Top 35 Medical writer Jobs in Massachusetts

Medical Writer (Remote, US)
Maquet Cardiovascular LLC —Boston, MA
- $105,000 - $115,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- 3 years
- Commuter assistance
- Disability insurance
Analyst/Medical Writer
Costello Medical —Boston, MA
- $71,000 - $76,500 a year
- Online Application
- Hybrid work
- Microsoft Excel
- No experience needed
- English
- Health insurance
- Dental insurance
Quick Apply
Medical Policy Writer
Cohere Health —Boston, MA
- $80,000 - $100,000 a year
- Remote
- Nursing
- Research
- Mid-level
- Paid parental leave
- Health savings account
Quick Apply
Medical Writer II
Laborie Medical Technologies Corp —Westborough, MA
- $115,000 - $120,000 a year
- Full-time
- 5 years
- English
- Microsoft Office
- Dental insurance
- Paid time off
Quick Apply
Senior Medical Writer- Clinical Focus
Veristat —Massachusetts
- $116,000 - $128,000 a year
- Full-time
- Remote
- Microsoft Word
- 3 years
- Bachelor's degree
- Paid holidays
- Tuition reimbursement
Associate Director-Medical Writer
Eli Lilly —Boston, MA
- $127,500 - $187,000 a year
- Full-time
- Microsoft Excel
- Management
- Master's degree
- Health insurance
- Dental insurance
Principal Medical Writer - Nonclinical Focus
Veristat —Massachusetts
- $132,000 - $151,000 a year
- Full-time
- Remote
- Microsoft Word
- 7 years
- Bachelor's degree
- Paid holidays
- Health insurance
6d
Principal Medical Writer-nonclinical focus
Veristat —Massachusetts
- $132,000 - $151,000 a year
- Full-time
- Remote
- Microsoft Word
- 7 years
- Bachelor's degree
- Paid holidays
- Health insurance
Senior Scientific Associate / Senior Medical Writer - Promotional Medical Writing (CST)
Precision AQ —Boston, MA
- $75,000 - $122,500 a year
- Online Application
- Remote
- Bachelor of Science
- Research
- Mid-level
Quick Apply
Senior Medical Writer - clinical focus
Veristat —Massachusetts
- $116,000 - $128,000 a year
- Full-time
- Remote
- Microsoft Word
- Mid-level
- 3 years
- Paid holidays
- Health insurance
Principal Medical Writer - Clinical Focus
Veristat —Massachusetts
- $142,000 - $153,000 a year
- Full-time
- Remote
- 7 years
- English
- Bachelor's degree
- Paid holidays
- Health insurance
10d
Director, Medical Writing
Alkermes, Inc. —Waltham, MA
- Full-time
- Management
- Psychiatry
- Doctor of Philosophy
Global Head, Medical Writing
Merck KGaA —Billerica, MA
- $234,800 - $352,200 a year
- Hybrid work
- 11+ years
- Master's degree
- Doctor of Philosophy
- Health insurance
- Paid time off
Associate Director / Director - Medical Writing, Oncology
Treeline Biosciences —Watertown, MA
- $164,450 - $224,787 a year
- Remote
- 8 years
- Bachelor's degree
- Doctor of Philosophy
Quick Apply
4d
Senior Medical Writer
Centessa Pharmaceuticals —Boston, MA
- $135,000 - $180,000 a year
- Full-time
- Microsoft Word
- Project management
- Doctor of Philosophy
- Wellness program
- Health insurance
Principal Medical Writer- MedPubs Focus
Veristat —Massachusetts
- $132,000 - $151,000 a year
- Full-time
- Remote
- 7 years
- Analysis skills
- Bachelor's degree
- Paid holidays
- Health insurance
Senior Medical Writing Manager
Grove —Boston, MA
- $70 - $76 an hour
- Full-time
- Word processing
- Computer literacy
- Writing skills
Quick Apply
Associate Director, Medical Writing
Alkermes, Inc. —Waltham, MA
- Full-time
- Doctoral degree
- Psychiatry
- Neurology
Associate Director, Medical Writing
Rhythm Pharmaceuticals —Boston, MA
- $160,000 - $240,000 a year
- Full-time
- Office
- Bachelor's degree
- Travel
Consultant I, Medical Writing
Syner-G —Boston, MA
- Hybrid work
- Microsoft Excel
- Mid-level
- Office
- Paid holidays
- Paid time off
Quick Apply

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medical writer jobs near massachusetts

Medical Writer (Remote, US)

Maquet Cardiovascular LLC -
Boston, MA

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Job Details

$105,000 - $115,000 a year

Benefits

Commuter assistance
Caregiver leave
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
401(k) matching
Life insurance

Qualifications

Search engines
Medical writing
Microsoft Outlook
PubMed
EndNote
ICH guidelines
Risk management
Biomedical regulatory compliance
Managing projects
Clinical quality assurance standards
ISO 13485

Full Job Description

Date: Aug 5, 2026

Location:
Boston, MA, US

Company: Maquet Cardiovascular LLC
Remote Work: 5 days at home (fully remote)
Salary Range: $105,000 - $115,000 10% STI

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

Job Overview

Responsible for the generation and development of documents relating to clinical evaluations and clinical investigations.

This position is hybrid or fully remote in the US preferably on EST zone.

This is a fixed term position with direct hire with Getinge with a high potential to convert to regular hire.

Job Responsibilities and Essential Duties

Serves as a clinical evaluation lead and participates within the clinical evaluation team for the development and generation of Clinical Evaluation Reports (CER) and associated documentation. Specifically contributes to the planning, literature review and the identification, appraisal and analysis of clinical data related to the evaluation in accordance to MEDDEV 2.7/1 Revision 4 and in alignment with EU MDR. Contributes to the Summary of Safety and Clinical Performance in alignment with EU MDR.
Serves as point and participates in the Post-Market Clinical Follow-up (PMCF) team. Specifically contributes to the literature review and the identification and analysis of clinical data related to the PMCF evaluation.
Performs comprehensive systematic, documented literature reviews using various search engines in order to support the Clinical Evaluation, Post-market Clinical Follow-Up, awareness of current State of the Art as well as protocol development and any ad hoc reports required. (20%)
Analyzes available clinical evidence (data held by the manufacturer, published literature) to assist the Clinical Affairs team with clinical development strategy.
Writes and or edits clinical study documentation, including clinical investigational plans/protocols, Investigator’s Brochures, Periodic reports, Clinical Investigational Reports/Clinical Study Reports. Ensure high quality study documentation that is submission-ready for various regulatory agency and external distribution.
Serves as a subject matter expert on clinical aspects of Technical documentation.
Writes and/or supports the development of manuscripts relating to clinical study data or clinical evidence for submission to peer-reviewed medical journals. Works with medical professionals to ensure alignment with journal requirements for targeted manuscript submission.
Writes and/or contributes to abstracts and submissions of clinical data to various medical congresses or symposia. Work with medical professionals to ensure high quality submissions and data integrity.
Contributes to the development and optimization of Clinical Affairs SOPs.
Performs other non-routine duties as assigned.

Required Knowledge, Skills and Abilities

Bachelors Degree in a relevant scientific discipline, or equivalent combination of education and experience.
A minimum of 3 years medical writing experience. Direct experience working on clinical evaluations within the Medical Device industry a plus.
Medical writing certification a plus.
A high level attention to detail and the ability to own and drive accuracy.
Strong interpersonal and communication skills.
Excellent project management skills with the ability to deliver projects on timelines that support corporate and departmental goals and objectives.
Strong analytical and organizational skills as well as demonstrated ability to solve problems with innovative solutions
Outstanding oral and written communication skills.
Proficiency in using and navigating PubMed, Embase and other literature search engines. Experience in DistillerSR, EndNote and other literature review tools a plus.
Strong working knowledge of regulations and guidance relating to Clinical Affairs, including EU MDR (2017/745), EU MDD (93/42/EEC), MEDDEV guidance, including 2.7/1 Revision 4 and 2.12/2 Revision 2, relevant MDCG guidance, ISO 14155, ICH guidance including E3 CSR, E6 (R3) GCP, and familiarity regulations/ guideline relating to Risk management (i.e. ISO 13485 and ISO14971)
Demonstrated ability to work independently and as part of a team.
Ability to interact with physicians in a professional manner.
Ability to prioritize tasks in a fast-paced environment. Ability to work under urgent deadlines and flexibility to accommodate fluctuating timelines.
Advanced skills using Microsoft Office products such as Outlook, Word, Excel and Power Point.
Travel requirements depending on projects.

Internal and External Contacts/Relationships

Internal Getinge teams such as Medical Affairs, Regulatory Affairs, Quality Engineering, Research & Development and Marketing, as needed.
External teams such as CROs, clinical vendors and key opinion leaders.

The base salary for the position is a minimum of $105,000 and a maximum of $115,000
#LI-JF1 #LI-remote

About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:

Health, Dental, and Vision insurance benefits
401k plan with company match
Paid Time Off
Wellness initiative & Health Assistance Resources
Life Insurance
Short and Long Term Disability Benefits
Health and Dependent Care Flexible Spending Accounts
Commuter Benefits
Parental and Caregiver Leave
Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

Nearest Major Market: Boston

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Refine Your Search

medical writer jobs in massachusetts

Medical Writer (Remote, US)

Analyst/Medical Writer

Medical Policy Writer

Medical Writer II

Senior Medical Writer- Clinical Focus

Associate Director-Medical Writer

Principal Medical Writer - Nonclinical Focus

Principal Medical Writer-nonclinical focus

Senior Scientific Associate / Senior Medical Writer - Promotional Medical Writing (CST)

Senior Medical Writer - clinical focus

Principal Medical Writer - Clinical Focus

Director, Medical Writing

Global Head, Medical Writing

Associate Director / Director - Medical Writing, Oncology

Senior Medical Writer

Principal Medical Writer- MedPubs Focus

Senior Medical Writing Manager

Associate Director, Medical Writing

Associate Director, Medical Writing

Consultant I, Medical Writing

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