Medical Writer (Remote, US)
Boston, MA · On-site +1
This position is hybrid or fully remote in the US preferably on EST zone. This is a fixed term ... Writes and or edits clinical study documentation, including clinical investigational plans ...
Medical Writer (Remote, US)
Boston, MA · On-site +1
This position is hybrid or fully remote in the US preferably on EST zone. This is a fixed term ... Writes and or edits clinical study documentation, including clinical investigational plans ...
Medical Writer (Remote, US)
Boston, MA · On-site +1
This position is hybrid or fully remote in the US preferably on EST zone. This is a fixed term ... Writes and or edits clinical study documentation, including clinical investigational plans ...
Medical Writer (Remote, US)
Boston, MA · On-site +1
This position is hybrid or fully remote in the US preferably on EST zone. This is a fixed term ... Writes and or edits clinical study documentation, including clinical investigational plans ...
Boston- Freelance Writer
Boston, MA · Remote
$100 - $2.0K/mo
This is a remote position. Calling All Local Experts: Get Paid to Share Your Family Adventures! Do ... Craft engaging articles about the best playgrounds, kid-friendly cafes, and weekend events in your ...
Quick apply
Boston- Freelance Writer
Boston, MA · Remote
$100 - $2.0K/mo
This is a remote position. Calling All Local Experts: Get Paid to Share Your Family Adventures! Do ... Craft engaging articles about the best playgrounds, kid-friendly cafes, and weekend events in your ...
Narrative Writer
Wakefield, MA · Remote
My Client is in need of a Clinical Narrative Writer ... The position is a 3 month, 40 hour a week REMOTE engagement. The therapeutic areas include ...
Narrative Writer
Wakefield, MA · Remote
My Client is in need of a Clinical Narrative Writer ... The position is a 3 month, 40 hour a week REMOTE engagement. The therapeutic areas include ...
Technical Writer II / Method Validation documents / Remote work Duration: 12 months contract, extendable up to 48 months Location: Remote Worker Note: The client has the right-to-hire you as a ...
Quick apply
Technical Writer II / Method Validation documents / Remote work Duration: 12 months contract, extendable up to 48 months Location: Remote Worker Note: The client has the right-to-hire you as a ...
Technical Writer/Editor (REMOTE)
Boston, MA · Remote
$60K/yr
Our writers create polished, thoughtful appraisal reports about companies in a wide variety of industries. No extensive business or financial experience is required - we'll provide all the training ...
Quick apply
Technical Writer/Editor (REMOTE)
Boston, MA · Remote
$60K/yr
Our writers create polished, thoughtful appraisal reports about companies in a wide variety of industries. No extensive business or financial experience is required - we'll provide all the training ...
Technical Writer
Lexington, MA · On-site +1
$69K - $158K/yr
Remote Work: Hybrid Job Number: R0241561 Location: Lexington,MA,US Share job via: Share Technical Writer The Opportunity: Write and edit technical documentation, user manuals, and sales and training ...
Technical Writer
Lexington, MA · On-site +1
$69K - $158K/yr
Remote Work: Hybrid Job Number: R0241561 Location: Lexington,MA,US Share job via: Share Technical Writer The Opportunity: Write and edit technical documentation, user manuals, and sales and training ...
Senior Writer
Boston, MA · On-site +1
$118K - $196K/yr
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Senior Writer
Boston, MA · On-site +1
$118K - $196K/yr
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Senior Writer
Boston, MA · On-site +1
$118K - $196K/yr
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Senior Writer
Boston, MA · On-site +1
$118K - $196K/yr
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Senior Writer
Boston, MA · On-site +1
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Quick apply
Senior Writer
Boston, MA · On-site +1
Please provide 2-3 writing samples of no more than 10 pages total, including a short screenplay ... Remote roles in the US are only available to candidates that reside in the following states:
Sr. Medical Writer
Mansfield, MA · On-site +1
Remote candidates are an option. Local candidate to Mansfield, MA preferred. Essential functions: * This role predominantly focuses on writing, editing and reviewing regulatory (e.g. Clinical ...
Sr. Medical Writer
Mansfield, MA · On-site +1
Remote candidates are an option. Local candidate to Mansfield, MA preferred. Essential functions: * This role predominantly focuses on writing, editing and reviewing regulatory (e.g. Clinical ...
Freelance Medical Writer
Belmont, MA · Remote
$50 - $75/hr
Custom Learning Designs has partnered with Hueman to find a Technical Writer - Freelance, remote. Custom Learning Designs (CLD) is a leading provider of custom training solutions for pharmaceutical ...
Quick apply
Freelance Medical Writer
Belmont, MA · Remote
$50 - $75/hr
Custom Learning Designs has partnered with Hueman to find a Technical Writer - Freelance, remote. Custom Learning Designs (CLD) is a leading provider of custom training solutions for pharmaceutical ...
Senior Technical Writer
Boston, MA · Remote
About the role We're looking for a Senior Technical Writer who brings craft and strategic instinct ... Remote, with a preference for the US East Coast time zone
Senior Technical Writer
Boston, MA · Remote
About the role We're looking for a Senior Technical Writer who brings craft and strategic instinct ... Remote, with a preference for the US East Coast time zone
Technical Writer (6-month contract)
Boston, MA · On-site +1
$35.58 - $40.87/hr
This position is a full-time, remote contract role with an expected duration of 6 months . As a contract position, it is not eligible for company-sponsored benefits . As a Technical Writer your day ...
Technical Writer (6-month contract)
Boston, MA · On-site +1
$35.58 - $40.87/hr
This position is a full-time, remote contract role with an expected duration of 6 months . As a contract position, it is not eligible for company-sponsored benefits . As a Technical Writer your day ...
Technical Writer (6-month contract)
Boston, MA · Remote
$35.58 - $40.87/hr
This position is a full-time, remote contract role with an expected duration of 6 months . As a contract position, it is not eligible for company-sponsored benefits . As a Technical Writer your day ...
Technical Writer (6-month contract)
Boston, MA · Remote
$35.58 - $40.87/hr
This position is a full-time, remote contract role with an expected duration of 6 months . As a contract position, it is not eligible for company-sponsored benefits . As a Technical Writer your day ...
Technical Writer
Gloucester, MA · Remote
$65K - $75K/yr
Axiom Consultants, Inc, is seeking a skilled Technical Writer to work closeley with the Project Manager to create appropriate project documentation for NOAA Fisheries Greater Atlantic Regional ...
Quick apply
Technical Writer
Gloucester, MA · Remote
$65K - $75K/yr
Axiom Consultants, Inc, is seeking a skilled Technical Writer to work closeley with the Project Manager to create appropriate project documentation for NOAA Fisheries Greater Atlantic Regional ...
Medical Writer - India (56829)
Boston, MA · On-site +1
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
Medical Writer - India (56829)
Boston, MA · On-site +1
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
Academic Writer/Editor
Boston, MA · On-site +1
$70K - $86K/yr
This position's work location is fully remote with the ocassional time onsite as needed. The ... The Academic Writer/Editor I manages the organization and execution of content, timelines, and ...
Academic Writer/Editor
Boston, MA · On-site +1
$70K - $86K/yr
This position's work location is fully remote with the ocassional time onsite as needed. The ... The Academic Writer/Editor I manages the organization and execution of content, timelines, and ...
Senior Principal Medical Writer
Billerica, MA · On-site +1
$126K - $215K/yr
As the Senior Principal Medical Writer, you will lead the end-to-end development of complex ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...
Senior Principal Medical Writer
Billerica, MA · On-site +1
$126K - $215K/yr
As the Senior Principal Medical Writer, you will lead the end-to-end development of complex ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...
Remote Weekend Writer information
See Boston, MA salary details
$16.71 - $21.03
9% of jobs
$25.28 is the 25th percentile. Wages below this are outliers.
$21.03 - $25.36
16% of jobs
$25.36 - $29.68
23% of jobs
The median wage is $30.27 / hr.
$29.68 - $34
12% of jobs
$34 - $38.32
3% of jobs
$38.32 - $42.64
2% of jobs
$42.64 - $46.96
4% of jobs
$46.96 - $51.28
1% of jobs
$53.90 is the 75th percentile. Wages above this are outliers.
$51.28 - $55.60
7% of jobs
$55.60 - $59.92
19% of jobs
$59.92 - $64.24
3% of jobs
$16
$38
$64
How much do remote weekend writer jobs pay per hour?
As of Aug 4, 2026, the average hourly pay for remote weekend writer in Boston, MA is $38.15, according to ZipRecruiter salary data. Most workers in this role earn between $25.34 and $55.38 per hour, depending on experience, location, and employer.
What is the difference between Remote Weekend Writer vs Remote Part-Time Content Creator?
| Aspect | Remote Weekend Writer | Remote Part-Time Content Creator |
|---|---|---|
| Credentials | Writing experience, portfolio, sometimes specific niche expertise | Similar writing skills, often with additional multimedia or social media skills |
| Work Environment | Primarily remote, flexible hours, weekend-focused | Remote, flexible hours, may include weekdays or weekends |
| Employer & Industry Usage | Media outlets, blogs, online publications | Brands, marketing agencies, online platforms |
| Search & Comparison Intent | Focus on weekend-specific writing roles | Broader content creation roles including multimedia |
The Remote Weekend Writer typically focuses on producing written content during weekends for online publications or blogs, requiring strong writing skills and niche expertise. The Remote Part-Time Content Creator may create various types of content, including videos, social media posts, and articles, often with a broader skill set. Both roles are remote and flexible but differ mainly in scope and content type.
What are popular job titles related to Remote Weekend Writer jobs in Boston, MA? For Remote Weekend Writer jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Remote Weekend Writer jobs in Boston, MA look for? The top searched job categories for Remote Weekend Writer jobs in Boston, MA are:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 29 days ago
Getinge rating
9.3
Based on 14 frontline employees who took The Breakroom Quiz
10th of 487 rated machine equipment manufacturers
Job description
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
Required Knowledge, Skills and Abilities
Internal and External Contacts/Relationships
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:
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.
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.
About Getinge
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
10,000+ Employees
Headquarters location
Dr Wayne, NJ, US