Scientific Writer Jobs in the United States
HTC Global Services Inc
Remote, OR
Develop comprehensive training materials — including user guides, e-learning content, and quick-reference documentation — that effectively communicate platform functionality to clinical end-users. In this role, you will help shape a new healthcare platform by translating oncology workflows, scientific evidence, and clinical requirements into product guidance, training content, and high-quality scientific publications.
Black Diamond Networks
Boston, MA
The role requires strong experience with MadCap Flare and structured content development, including reusable content strategies, variables, condition tags, and multi-channel publishing outputs. JOB SCOPE: The Technical Writer will be responsible for authoring, revising, and maintaining end-user documentation for medical devices in compliance with applicable regulatory and quality system requirements.
Talent Software Services
$55 - $61.75
North Wales, PA
Previous involvement with creating materials for Medical Information/Field Medical Personnel, including but not limited to medical information letters, slide decks, frequently asked question (FAQ) documents; not looking for SOP or regulatory document writing experience. In this position, you will be responsible for: Creating new/updating Medical information letters, Slide decks, and FAQs according to the release of new data and monthly expiration reports and sending them through the review and approval process.
Mindlance
$42 - $50
Atlanta, GA
Top 3/5 Skills: Technical Writing (Life Sciences / Medical Devices), Knowledge of IVD / Medical Devices, Understanding of industry regulations & compliance (governance requirements), Documentation skills. · May be asked to troubleshoot complex problems and engages others in problem-solving strategies to identify practical and effective solutions to complex issues.
Techlink Systems Inc
$42 - $45
Little Canada, MN
You will collaborate with product managers, engineers, UX, QA, and other business stakeholders to refine and deliver requirement specifications and other software project deliverables—transforming complex technical concepts into concise, well-organized, and audience friendly documents. Bachelor’s degree in Technical Communication, Engineering, Computer Science, Biomedical Engineering, Systems Engineering, or relevant field; Clear understanding of software development processes (SDLC).
Jazz Pharmaceuticals
$196000 - $294000
Philadelphia, PA
In collaboration with key stakeholders within medical affairs functions, lead the medical communication strategy activities at key medical congresses, including the medical and/or therapeutic area booth panel development, other booth materials, meeting summaries to internal audiences, and post-meeting slide reviews to internal audiences; ensure all materials undergo appropriate medical affairs review committee assessment. May serve as Business Process Owner, Document Owner, and/or Author of governance and procedural documents related to Jazz publication processes, including developing and updating documents as needed to reflect current processes, and overseeing documents through the appropriate stakeholder review and approval process.
Lancesoft Inc
$60 - $69
Ewing Township, NJ
The Contractor Medical Writer, Medical Information, Payer and Health Systems reports to the Associate Director/Director Med Info-PHS and supports the development and dissemination of Medical Information scientific content and materials to Payers, Healthcare Intermediaries and Health Systems across the assigned CLIENT portfolio of products. · Works closely with RW V&E Field, Medical Affairs Therapeutic Area team(s) and Medical Information Scientific Engagement Contact Center to guide creation and delivery of responses to unsolicited Medical Information Requests from Payers and Health Systems .
Applied Medical
$70000 - $80000
Rancho Santa Margarita, CA
The Associate Clinical Writer’s primary responsibilities are developing and completing scientific protocols and reports, including, but not limited to, Clinical Evaluations and Post Market Clinical Feedback as part of design validations for medical devices to support product registrations internationally. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.
Compose.ly
$115000 - $130000
undefined, undefined
The ideal candidate will have experience interpreting complex clinical and statistical data, crafting high-impact scientific manuscripts, and working with multiple key opinion leaders (KOLs). To support client's scientific communications efforts by developing high-quality manuscripts for peer-reviewed journals and abstracts for scientific conventions.
Compose.ly
$60 - $70
undefined, undefined
You'll bring deep therapeutic expertise (priority: hematology/oncology, plus non-malignant heme and rare diseases) and own end-to-end content development across digital, live virtual, and in-person HCP education. Our client bridges independent medical education and branded promotional work, delivering clinician-focused programs through a Scientific Services team comprising Medical Science Directors, Medical Writers/Editors, Creative, and Editorial.
Voloridge Health
JUPITER, FL
As a Scientific Content Writer Intern, you will work closely with research leadership to create knowledge documents that formally summarize and contextualize Voloridge Health’s internal research findings. Currently enrolled in an undergraduate or graduate program in Biology, Biochemistry, Biomedical Science, Public Health, Neuroscience, English (with scientific writing experience), or a related field .
TechDigital
New Brunswick, NJ
2. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the reports, in addition to reviewing DMPK regulatory documents, editing of nonclinical study reports for regulatory acceptance and adherence to company templates, SOPs, DMPK/BA methods, work practices and FDA GLPs, as applicable. Skills/Knowledge Required: • At minimum, a Bachelor's degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs.
B.E. Meyers & Co, LLC
$90000 - $105000
Redmond, WA
While working under moderate supervision, the Technical Writer is responsible for creating clear, accurate, and concise documentation to support production and engineering activities. Demonstrated ability to produce high-quality, clear, and concise documents including work instructions, assembly drawing for production and tooling, guides, and tutorials.
Medpace, Inc.
Cincinnati, Ohio
Qualifications : A minimum of a Bachelor's degree, with previous experience in a research laboratory; Writing communication prefered; Knowledge of GLP, cGMP, and ICH guidelines; Strong organizational and communication (written and oral) skills; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Department of Ecology
$58584 - $78912
Richland, WA
Ecology employees may be eligible for the following: Medical/Dental/Vision for employee & dependent(s), Public Employees Retirement System (PERS), Vacation, Sick, and other Leave, 11 Paid Holidays per year, Public Service Loan Forgiveness, Tuition Waiver, Long Term Disability & Life Insurance, Deferred Compensation Programs, Dependent Care Assistance Program (DCAP), Flexible Spending Arrangement (FSA), Employee Assistance Program, Commute Trip Reduction Incentives, Combined Fund Drive, SmartHealth *Click here for more information. You will collaborate with federal agencies, contractors, technical specialists, and local and regional partners; navigate the intricate and often complicated permitting history of Hanford facilities; and help resolve disagreements between Ecology and permittees as part of the permitting and oversight process.
Alliance Technical Group, LLC
Vancouver, WA
The primary duties of the Technical Services Writer include technical writing of proposals, test plans and reports for source testing projects. Draft reports are. then provided to the project manager or technical services manager for review prior to submittal to the clients.
Performance Development Group
Philadelphia, PA
Our network of consultants loves to work with us and here are some of the reasons why they find a relationship with PDG to be so valuable to them: Variety is the spice of life: PDG's wide variety of learning projects gives you the opportunity to be a part of the design and development of award-winning programs that help to move the needle on employee performance while enhancing your experience and skills. Collaborate with project/account managers, instructional designers, graphic artists, programmers, editors, and quality assurance specialists to ensure clients' needs are met and the end product is accurate and of high quality.
American Association for Cancer Research
Philadelphia, Pennsylvania
Overview: The science writer in the Communications and Public Relations Department is responsible for translating scientific data and information related to cancer research into content that helps educate the public, policymakers, media and the health care industry about cancer research advances, the AACR’s mission, and the importance of biomedical science and funding. Collaborating with SciComm members and media relations staff to help identify important cancer research advances from AACR’s journals, scientific conferences, programs, and other initiatives to communicate to the scientific/medical press, national press, policymakers, cancer research community, and the public.
Criterion Edge Professional Services Inc.
Los Angeles, CA
In the role of Medical Writer, you will have the opportunity to work closely with other writers, project managers and support specialists to produce a wide variety of regulatory and scientific reports, plans, and other written deliverables for medical device, pharma/biotech, and in vitro device clients. By leveraging best-in-class writing processes, technology, and experience, our expert team of writers and project managers support healthcare companies to achieve their global regulatory goals with superior quality, speed, and budget control.
CareQuest Institute for Oral Health Inc
$87000 - $102400
Boston, MA
The Science Writer I is part of the Analytics and Data Insights team and is responsible for writing, editing, and assisting with coordinating the production of publications (short- and long-form reports, white papers, and scientific journal articles), posters, and other presentations for CareQuest Institute for Oral Health. Under the direction of the Senior Director and in partnership with the Science Writer II, help plan, develop, and implement science and policy writing activities that elevate oral health, showcase CareQuest Institute’s programs and grant-making, and position the organization as a leading voice.
Octane Learning
Princeton, NJ
Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several different styles of training, primarily interactive media such as eLearning, instructor-led courses/workshops, videos, and print resources; and (2) medical communications activities such as advisory boards, symposia, and speaker slide decks For these materials, within the constraints of our/clients’ guidelines, you will: Review client’s goals and strategy . There will likely be opportunities for additional work in curriculum design, audit and gap analysis, content creation for marketing collateral, as well as learning strategy, as the workload presents, and your capacity/interest aligns.
Octane Learning
Princeton, NJ
Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several different styles of training, primarily interactive media such as eLearning, instructor-led courses/workshops, videos, and print resources; and (2) medical communications activities such as advisory boards, symposia, and speaker slide decks For these materials, within the constraints of our/clients’ guidelines, you will: Review client’s goals and strategy . There will likely be opportunities for additional work in curriculum design, audit and gap analysis, content creation for marketing collateral, as well as learning strategy, as the workload presents, and your capacity/interest aligns.
AdMed Inc.
Philadelphia, PA
AdMed is an award winning, integrated agency that designs and delivers modern training tools for pharmaceutical, biotech, diagnostic and medical products, with one goal: to ensure that healthcare professionals, sales teams, employees and consumers understand what they need to know regarding the science behind their products. The role involves all stages in the development of AdMed’s products – from brainstorming with clients, to researching and writing original content, to acting as a virtual teacher in video training programs.
Artech LLC
$50 - $55
Virtual, MN
Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. The majority of time is spent delivering and overseeing the projects from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.
Lumanity
Yardley, Pennsylvania
Responsibilities / Position overview: We are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical Strategy and Communications team, which serves our clients by mobilizing our scientific knowledge to interpret the data and create compelling narratives to guide their medical strategy and through regulatory challenges. The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts), slide decks, scientific platforms, symposia, advisory boards, and training materials.
AdMed Inc.
Philadelphia, PA
AdMed is an award winning, integrated agency that designs and delivers modern training tools for pharmaceutical, biotech, diagnostic and medical products, with one goal: to ensure that healthcare professionals, sales teams, employees and consumers understand what they need to know regarding the science behind their products. AdMed has over 30 years of industry experience and we are looking for a dynamic, passionate, experienced Assistant Medical Writer to join our team.
Parexel
Olympia, WA
Job Purpose: The Senior Medical Writer is responsible for the development of medical writing deliverables that support the clinical regulatory writing portfolio and works with guidance and oversight to achieve goals. Early Development/Translational Medical Writing experience required.
WebMD LLC
$85000 - $95000
New York, NY
An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; minimum of a Bachelor of Science degree (life sciences, public health, or clinical sciences) or similar with several years' relevant work experience required. Medscape Medical Affairs, a division of WebMD, is a trusted resource for physicians and healthcare professionals, offering clinical reference tools, the latest medical information, education, and peer-to-peer collaboration opportunities.
Criterion Edge Professional Services Inc.
Los Angeles, CA
In the role of Associate Medical Writer, you will have the opportunity to work closely with other writers, project managers and project support specialists to support and lead multiple PER writing projects that support EU IVDR submission requirements for the client’s portfolio of IVD products. Be on the leading edge by applying your regulatory writing expertise and leadership skills to the development, management and writing of regulatory-compliant performance evaluation reports (PER) projects with top industry clients.
Exploratorium
San Francisco, CA
Collaboration: Work closely with scientists, artists, developers, designers, visitor research and evaluation staff, project leaders, and senior science writers to develop and write content for exhibitions, digital projects, activities, and programs, and to articulate conceptual frameworks for exhibition projects, including organizational structures and storylines. Writing: Research, curate, propose, and vet scientific content; edit, interview, and consistently develop engaging, accurate, and current science content across a variety of projects, with mentorship from Lead Science Writers and the Editorial Department Manager or Director; make timely editorial decisions and exercise creative discernment in shaping ideas.
Blue Star Partners LLC
$40 - $45
Maple Grove, MN
Cross-Functional Collaboration: Partner with Sales, Marketing, R&D, Regulatory Affairs, Product Performance Group, Quality Engineering, Clinical Affairs, Clinical Science, Risk Management, and Medical Affairs to ensure comprehensive and accurate CER-related outputs. Document Authoring: Write and contribute to clinical evaluation reports, plans, post-market surveillance (PMS) and post-market clinical follow-up (PMCF) reports, summary of safety and clinical performance (SSCP) documents, and regulatory responses.
Blue Star Partners LLC
$65 - $75
Maple Grove, MN
Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables. Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), physician training materials, ensuring alignment of risk information.
Atria Physician Practice New York PC
$175000 - $200000
New York, NY
About Atria: Atria is a membership-based preventive health care practice delivering cutting-edge primary and specialty care in New York, South Florida, Los Angeles (2026), and through 24/7 telemedicine globally. Stay current with developments in preventive medicine, longevity research, and health care technology, identifying opportunities for Atria to provide valuable commentary and education on emerging trends.
Certara
Remote, undefined
Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization. Analytical skills and ability to understand and summarize a variety of data, including preclinical, clinical (phase 1-4), pharmacokinetic (PK), and pharmacodynamic data, experience with population PK and modeling data a plus.
GLE Creative Talent, Inc.
$100000 - $160000
New York, New York
Working closely with internal teams and clients, youll translate complex clinical data into clear, compelling narratives that support payer engagement and brand success. As a Medical Writer, Market Access, you will play a critical role in developing strategic, scientifically accurate content that drives brand differentiation and maximizes access goals.
Blue Star Partners LLC
$40 - $50
Maple Grove, MN
Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables. Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), physician training materials, ensuring alignment of risk information.
Prime
$85000 - $95000
New York, NY
This is defined by the Prime mission: Through a pioneering fusion of the finest expertise in science, strategy, evidence, technology and creativity we deliver the world-class outcomes that our global partners trust to achieve their goals. It speaks to the significant challenges that exist within global healthcare, and how we, as one team, can help to deliver better solutions and outcomes for our partners and for patients everywhere, sooner.
MMS
undefined, (Multiple States)
Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS
undefined, (Multiple States)
Write and edit clinical development documents, mostly focusing on clinical protocols but the overall role may include, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS
undefined, (Multiple States)
Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Medpace, Inc.
Cincinnati, Ohio
We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.
Lumanity
Yardley, Pennsylvania
This position falls within our wider Medical Strategy and Communications division, which serves our clients by mobilizing our scientific knowledge to interpret data and create compelling narratives to guide their medical communications strategy in the context of the current therapeutic landscape and through regulatory challenges. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated.
Lancesoft
$50
Lafayette, CO
Education and Experience Required: Baccalaureate degree in Life Sciences, Pharmacy, Medicine, Biomedical Engineering, or Public Health, ideally with training in Clinical Research or Regulatory Affairs. This role offers an exciting opportunity to work in a dynamic environment where you will contribute to the development and implementation of clinical evaluation documents in compliance with the European Union Medical Device Regulation (EU MDR).
Inotiv, Inc.
$56000 - $65000
Boulder, CO
Minimum Requirements * Bachelor's degree in science related discipline * Familiarity with writing and interpreting scientific reports and data * Demonstrated proficiency in Microsoft Office Suite (Outlook, Word, Excel) and Adobe Acrobat with ability to quickly learn and master new software applications as needed (Photoshop, InDesign, etc.) Preferred Qualifications * Prior report writing or Quality Cont ol/Quality Assurance experience * One year experience with data analysis in a research setting * One year experience in a regulated environment (FDA and/or GLP) Working Conditions & Physical Requirements The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. (The phrases occasionally, regularly, and frequently correspond to the following definitions: occasionally means up to one-third of working time, regularly means between one-third and two-thirds of working time, and frequently means two-thirds and more of worki General * Ability to read, write, speak and understand English Physical Activity * Moderate physical activity.
Crain Communications
Seattle, WA
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor s legal duty to furnish information. About Crain Communications: Crain Communications is a leading business news and information company with a portfolio of 24 media brands that provide indispensable coverage and data for professionals globally and across sectors, including advertising, automotive, finance, healthcare, staffing, and workforce solutions.
Climate Central
Princeton, NJ
Reporting to the vice president for content creation, the writer and associate producer will join an interdisciplinary team of communications professionals, writers, graphic designers, scientists, and technologists and will work across programs and projects at the organization. This person will help create reporting resources on a range of topics related to climate change impacts and solutions to help our network tell timely, relevant, and accurate stories about our warming planet.
MMS
Miami, FL
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide. Roles & ResponsibilitiesUnder minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
Biofire
$95000 - $124000
Salt Lake City, UT
In addition, bioMérieux offers a competitive Total Rewards package that may include: · A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options · Company-Provided Life and Accidental Death Insurance · Short and Long-Term Disability Insurance · Retirement Plan including a generous non-discretionary employer contribution and employer match. This role is responsible for developing clear, accurate, and scientifically sound documents that effectively communicate complex clinical, medical, and scientific data to healthcare professionals, internal stakeholders, and external audiences.
Systimmune
Princeton, NJ
The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.