Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. Expert ...
Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. Expert ...
Medical Writer
Bethesda, MD · On-site
Job Title Medical Writer Location Bethesda, MD 20817 US (Primary) Category Medical Writing Job Type Full-Time Salary Range 70,000.00-85,000.00/YEAR Education Master's Degree Travel None * Prepares ...
Medical Writer
Bethesda, MD · On-site
Job Title Medical Writer Location Bethesda, MD 20817 US (Primary) Category Medical Writing Job Type Full-Time Salary Range 70,000.00-85,000.00/YEAR Education Master's Degree Travel None * Prepares ...
Medical Writer
Woodcliff Lake, NJ · Hybrid
... international regulations, Client standards and processes, and the Client Writing Style Guide as ... The medical writer should be familiar with ICH guidelines and the current AMA Style Manual. The ...
Medical Writer
Woodcliff Lake, NJ · Hybrid
... international regulations, Client standards and processes, and the Client Writing Style Guide as ... The medical writer should be familiar with ICH guidelines and the current AMA Style Manual. The ...
Analyst/Medical Writer
Boston, MA · On-site
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
Quick apply
Analyst/Medical Writer
Boston, MA · On-site
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
Senior Medical Writer
Cambridge, MA · On-site
$134K - $162K/yr
Our clients include national and international biopharmaceutical and medical device companies of all sizes. RESPONSIBILITIES The Senior Medical Writer position requires writing and editing of ...
Quick apply
Senior Medical Writer
Cambridge, MA · On-site
$134K - $162K/yr
Our clients include national and international biopharmaceutical and medical device companies of all sizes. RESPONSIBILITIES The Senior Medical Writer position requires writing and editing of ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
The Principal Medical Writer will collaborate with internal teams to lead, write, and manage ... Maintain expert knowledge of US and international regulations, requirements, and guidance ...
Basking Ridge, New Jersey (Hybrid) Duration: 3-Month Contract with Potential for Full-Time Conversion Full-Time Contract Role: (40 hours/week) Our client is seeking an experienced Medical Writer to ...
Basking Ridge, New Jersey (Hybrid) Duration: 3-Month Contract with Potential for Full-Time Conversion Full-Time Contract Role: (40 hours/week) Our client is seeking an experienced Medical Writer to ...
Analyst/Medical Writer
Boston, MA · Hybrid
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
Analyst/Medical Writer
Boston, MA · Hybrid
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
... medical companies. As specialists in recognising talent we pride ourselves on not just finding the ... We encourage and reward knowledge sharing and have various support networks and international ...
... medical companies. As specialists in recognising talent we pride ourselves on not just finding the ... We encourage and reward knowledge sharing and have various support networks and international ...
Analyst/Medical Writer
Boston, MA · On-site
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
Analyst/Medical Writer
Boston, MA · On-site
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... international congresses, with the opportunity to provide on-site support at such events. In ...
Medical Writer
Lewisville, TX · On-site
Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...
Medical Writer
Lewisville, TX · On-site
Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...
Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...
Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...
Senior Medical Writer
Yardley, PA · On-site
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
Senior Medical Writer
Yardley, PA · On-site
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. * Expert ...
Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. * Expert ...
Senior Medical Writer
Yardley, PA · On-site
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
Senior Medical Writer
Yardley, PA · On-site
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the ... Working with leading international pharmaceutical clients, you will be interacting with some of the ...
Senior Medical Writer
Rockville, MD · On-site
Ensures that medical writing deliverables conform to the International Conference on Harmonization (ICH) and other relevant regulatory guidelines * Creates and maintains standard operating procedures ...
Senior Medical Writer
Rockville, MD · On-site
Ensures that medical writing deliverables conform to the International Conference on Harmonization (ICH) and other relevant regulatory guidelines * Creates and maintains standard operating procedures ...
Medical Writer Associate
Bethesda, MD · On-site
Job Title Medical Writer Associate Location Bethesda, MD 20817 US (Primary) Category Medical Writing Job Type Full-Time Salary Range 54,000.00-60,000.00/YEAR Education Bachelor's Degree Travel None
Medical Writer Associate
Bethesda, MD · On-site
Job Title Medical Writer Associate Location Bethesda, MD 20817 US (Primary) Category Medical Writing Job Type Full-Time Salary Range 54,000.00-60,000.00/YEAR Education Bachelor's Degree Travel None
International Medical Writer information
See salary details
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
How much do international medical writer jobs pay per hour?
As of Jun 15, 2026, the average hourly pay for international medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.
What does an International Medical Writer do?
An International Medical Writer creates and manages medical documents for global healthcare audiences, including regulatory authorities, healthcare professionals, and patients. They write clinical study reports, regulatory submissions, scientific publications, and medical communications while ensuring compliance with international guidelines. This role requires strong scientific knowledge, attention to detail, and the ability to communicate complex medical information clearly. They often collaborate with cross-functional teams, including researchers, clinicians, and regulatory experts.
What are the key skills and qualifications needed to thrive in the International Medical Writer position, and why are they important?
To thrive as an International Medical Writer, a solid background in life sciences or medicine, exceptional written English, and familiarity with global regulatory guidelines are essential. Competence with tools such as Microsoft Office Suite, reference management software, and submission platforms like CTD/eCTD is often required; certification from organizations like AMWA or EMWA can be advantageous. Strong cross-cultural communication, attention to detail, and the ability to manage multiple projects under tight deadlines set top performers apart. These skills ensure the production of accurate, compliant medical documents that meet the diverse standards of international clients and regulatory bodies.
What does a typical workday look like for an International Medical Writer?
A typical day for an International Medical Writer involves researching scientific literature, drafting and editing regulatory or clinical documents, and collaborating virtually with cross-functional teams across different countries. You may participate in meetings with clients or internal stakeholders to clarify project requirements and timelines. Reviewing feedback, ensuring consistency with regional guidelines, and managing multiple assignments are also part of the routine. The role often requires balancing independent work with frequent communication and collaboration to ensure accuracy and timely project delivery.
More about International Medical Writer jobs
What are the most commonly searched types of International Medical Writer jobs? The most popular types of International Medical Writer jobs are:
What job categories do people searching International Medical Writer jobs look for? The top searched job categories for International Medical Writer jobs are:
Job description
Company Description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Position Title: Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project Manager Job Function Summary The Medical Writer Specialist is responsible for preparation of documents that support the presentation and/or publication needs of assigned therapeutic areas and/or medical devices in the DePuy Synthes Strategic Medical Affairs Team for a wide range of audiences. Key Job Activities: Primarily focuses on preparing, writing, editing, and reviewing regulatory (e.g. Clinical Evaluation Reports (CERs), clinical data reports or summaries) documents and responses to regulatory authorities (e.g. notified bodies).
Participates in post-market surveillance activities by conducting routine systematic literature reviews (e.g. screens articles against inclusion/exclusion criteria, extracts data from included studies, interprets study results, synthesizes literature, and prepares summaries into formal reports) for specific medical device groups or sub-groups. Performs scientific writing (e.g. abstracts, manuscripts, presentations). Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. Ensures documents are produced in accordance with procedures, internal and external guidelines (e.g. MEDDEV 2.7.1), and electronic templates. Ability to quickly acquire understanding of therapeutic areas, medical device portfolios, business objectives, clinical data/evidence Independently, critically writes and edits scientifically complex documents for substantial intellectual content. Reviews and provides input on clinical data being considered for presentation and/or publication to ensure alignment with scientific strategies and corporate goals. Expert knowledge of clinical research, device/drug development processes, regulatory requirements, good clinical and data management practices. Ability to understand and interpret statistical results of clinical studies; specifically summarize complex results and present them in clear, concise, and scientifically accurate manner to various end users. Communicates with various departments (e.g. Regulatory, Product Development, Clinical Research, Quality) to identify the necessary clinical and technical information.
Qualifications
Education Ph.D. /Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g. medical writing, regulatory affairs, clinical research, engineering)
BS/B.Pharm/BSN or MS or MPH plus 4 to 5 years of relevant medical device/drug industry experience Knowledge/Requirements
Excellent English language skills, especially writing and proofreading.
 Clinical, scientific or research background, highly preferred.
 Experience writing CERs, highly preferred.
 Knowledge in narrative or systematic literature reviews (e.g. PRISMA, Cochrane), highly preferred.
 Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred.
 Expert understanding of scientific or clinical research and methods.
 Understanding of statistical data and good data management practices.
Strong oral communication, presentation, project management and prioritization skills.
 Excellent interpersonal relationships.
Highly proficient in Microsoft Office Suite and bibliographic software (e.g. Endnote, Reference Manager).
Additional Information
All your information will be kept confidential according to EEO guidelines.
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996