192 Results for

Science Writer Jobs in the United States

Jobs

New!

Burlington, VT5 days ago

$80,600–$145,000 Per Year

Discover what your 25,000 future colleagues already know: Why Syneos Health* We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.* Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables.

New!

Warren, MI6 days ago

Level of proficiency with Teamcenter, Vis Mockup, and Arbortext is expected at the start- would take experience at a dealership or auto repair than being knowledgeable in this area. CAD Visualization & Graphic Creation: Proficiency with Teamcenter and Vis Mockup for creating graphics from math data.

7 days ago

Remote

Candidate shall possess a bachelor's degree in the following area of studies or similar subjects: Project management, Engineering, Computer Science, Information Science or Systems or other applicable technical discipline. Budget Tracking G Reports: Monitor project budgets, track expenditures, and prepare financial reports to ensure alignment with funding allocations and cost controls.

New!

Glenwood Springs, CO4 days ago

What once started in a barn, and grew to offering several different product lines, has now led us to where we are today, a full-service John Deere Dealership Team. Company DescriptionWe started as a small, barn-based repair and welding service in Parker, Colorado in 1977, and blossomed into Potestio Brothers Equipment, Inc.

New!

The Lakes, NVToday

Remote

This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive experience authoring Clinical Study Reports (CSRs), protocols, and regulatory submission documents across Phase I III studies. The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams.

New!

New Brunswick, NJ1 day ago

$42.85–$45.45 Per Hour
Full-time
Employee

Responsibilities:Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.

Lacey, WA8 days ago

$75,108–$100,980 Per Year
Full-time
Employee

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. Ecology seeks diverse applicants: We view diversity, equity, inclusion, and respect through a broad lens including race, ethnicity, class, age, religion, sexual orientation, gender identity, immigration status, military background, language, education, life experience, physical disability, neurodiversity, and intersectional identities.

Seattle, WA22 days ago

Full-time
Employee

Contributes to the project strategy to meet target goals and milestones, evaluates resource allocation needs, and monitors project risks to determine the best mitigation path. For non-sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms.

Philadelphia, Pennsylvania30+ days ago

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.

Alexandria, Virginia30+ days ago

EDJ Associates, Inc. is a Woman-Owned Small Business (WOSB) providing trusted communications, writing, digital, and program support services to federal agencies. This role focuses on producing accessible, engaging content for web, video, and audio platforms that communicate NSF programs and research impacts.

30+ days ago

We're looking for contributors with subject matter expertise in Earth Science, Biology, Physics, Astronomy, and Chemistry (and their sub-disciplines) to produce high-quality posts on recent discoveries/research, as well as guides and outlining content for infographics. It does mean that you're familiar with the leading academic journals in the subject and have the background knowledge to understand the significance of new research.

Saint Paul, MN30+ days ago

Full-time

You will work independently on larger, moderately complex projects, contributing to project milestones and collaborating with cross-functional teams. Required Knowledge and Experience Baccalaureate degree or equivalent, with a minimum of 2 years of relevant experience, or an advanced degree with no experience required.

Washington D.C, DC30+ days ago

With subject matter expertise in all-source analysis, mission support services, and information technology, we provide tailored solutions that address both major strategic challenges and day-to-day operational needs. Human Capital Resources and Concepts Inc. (HCRC) is a consulting firm specializing in comprehensive resource management solutions supporting federal organizations.

Mounds View, MN30+ days ago

Full-time

HM's Top Needs: Experience with peer-reviewed manuscript development from clinical research/studies Strong writing skills Project management Education Required: Bachelor’s Years’ Experience Required: 4 years (or 2 with advanced degree) Work Schedule: 40 hours a week Work Location: Mounds View On-site Requirement: Yes, 4 days starting in September Responsibilities Lead publication plan development and produce scientific content aimed at external audiences to maximize awareness and accessibility. Support team activities at medical device congresses, as assigned, which may include attending publication planning meetings with investigators in *** clinical trials, executing *** sponsored symposia, and covering relevant scientific sessions.

New York, NY30+ days ago

$175,000–$200,000

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.

New!

The Lakes, NV1 day ago

Remote

Seattle, WA23 days ago

Full-time
Employee

Eight (8) or more years of experience as a business analyst, project coordinator, project manager, business manager, technical writer, technical support, or systems analyst, required. The Business Analyst Senior Manager, Digital Transformation & Innovation (DT&I) plays a pivotal role in driving the strategic initiatives that enhance our digital capabilities.

San Diego, CA30+ days ago

$100,000–$150,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

Philadelphia, PA30+ days ago

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.

Yardley, Pennsylvania30+ days ago

Remote

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.

Los Angeles, CA30+ days ago

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.

New!

NULL, NULL1 day ago

RESPONSIBILITIES: Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator s brochures and periodic safety reports (PBRERs, DSURs, etc.) Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries). Base Salary - USD $142,100 to $195,360*** Never repost ***Full-timeBenefits - FullRelocation Assistance Available - NoCommission Compensation - NoBonus Eligible - NoOvertime Eligible - NoInterview Travel Reimbursed - NoCandidate Details7+ to 10 years experienceSeniority Level - Mid-SeniorManagement Experience Required - NoMinimum Education - Bachelor's DegreeWillingness to Travel - NeverScreening Questions.

Philadelphia, PA30+ days ago

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.

Philadelphia, PA30+ days ago

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.

Los Angeles, CA30+ days ago

Full-time

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.

Paramus, 076527 days ago

The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents. Regulatory Document Writing:Prepare and author clinical and regulatory documents, including but not limited to:Clinical Study Protocols (CSPs) and Protocol Amendments.

Cincinnati, Ohio30+ days ago

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.

30+ days ago

$60–$70

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.

New York, NY30+ days ago

$85,000–$95,000

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.

(Multiple States)30+ days ago

Remote

Full-time

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.

(Multiple States)30+ days ago

Full-time

(Multiple States)30+ days ago

Full-time

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.

Paramus, NJ7 days ago

Princeton, NJ30+ days ago

Full-time

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.

Princeton, NJ30+ days ago

Full-time

Austin, TX30+ days ago

The role will partner closely with technical teams and business stakeholders to translate system functionality, workflows, and processes into clear, user-friendly documentation. This position will function as a Business Systems Analyst with a strong focus on technical writing and end-user documentation in support of the newly integrated Maximo system.

Fort Leavenworth, KS30+ days ago

This role focuses on crafting realistic cyber operational environments, including offensive and defensive cyberspace operations, to enable training units to effectively meet their training objectives during Warfighter Exercises (WFX) and other mission command events. Collaborate with US Army Cyber Command (ARCYBER) to ensure scenario fidelity by integrating current intelligence and real-world cyber threats into training events, enhancing the realism and complexity of the simulated cyber environment.

Chicago, IL30+ days ago

Remote

Full-time

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.

Lafayette, CO30+ days ago

Full-time

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).

New!

Princeton, NJ4 days ago

Full-time

Reporting to the Vice President for Content Creation, this person will work across teams and projects alongside writers, designers, scientists, technologists, and communications professionals to help create timely, accurate, and engaging climate change content. This role supports Climate Central’s editorial, creative, and communications work through science writing, cross-team editorial support, production coordination, and quality assurance.

Buffalo Grove, IL8 days ago

$35–$38 Per Hour

This role will work closely with engineers, developers, product managers, and subject matter experts to develop documentation including user guides, SOPs, work instructions, installation manuals, and training materials. Must have Skill Set: Technical writing experience, strong written communication skills, Microsoft Office proficiency, attention to detail, ability to work cross-functionally with technical teams.

Nutley, NJ13 days ago

$42–$47 Per Hour
Contractor

Title: SOP Writer Location: Nutley, NJ- Hybrid Duration: 12 Months+ Possible Extension Pay Range: $42- $47/hr Requirements Bachelors degree in English or related subject, or Bachelors degree in science with proven writing experience. Experience of working with multiple disciplines in clinical development in the pharmaceutical industry, with knowledge of the drug development process.

Warren, MI9 days ago

$27–$30

Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. Summary: The main function of a Technical Writer is to write technical materials, such as equipment materials, appendices, or operating and maintenance instructions.

Springfield, VA30+ days ago

$39,000–$40,000 Per Year

In this role, you'll provide vital proposal development, technical writing, data analysis, price analysis, competitive business intelligence utilizing top technical tools such as GOVWIN, GOVTRIBE, and SAM.Gov. Comprehensive understanding of MS Office Suite and Google Apps- Ability to establish and maintain effective working relationships with executive management, peers, employees, clients, other agencies, and the public.

San Diego, CA30+ days ago

What powers their growth across Breast & Skeletal Health, Diagnostic Solutions, and GYN Surgical Solutions is also what differentiates them: the exceptional and clinically proven ability of their products to detect, diagnose, and treat illnesses and other health conditions earlier and better. Their proficiency and commitment to develop and share more robust, science-based certainty drives the company's increasingly global presence, as well as a pipeline that responds to the unmet health and wellness needs of women, families, and communities.

Birmingham, AL19 days ago

As part of the Companys Power Delivery Data Analytics team, the Communication and Documentation Specialist serves a multifunctional role focused on internal communications and technical documentation and supports existing internal communications and documentation team. ** Johnson Service Group (JSG) is a nationally recognized professional staffing and recruiting firm that is looking for an experienced Technical Writer to fill a contract assignment in the Birmingham, Alabama area.

Oak Ridge, TN19 days ago

Akima Infrastructure Services, LLC (AIS), is actively seeking Engineering, Professional, Technical, and administrative support personnel as part of our staff augmentation team supporting the Department of Energy at the Y‑12 National Security Complex located in Oak Ridge, Tennessee and the Pantex Plant located in Amarillo, Texas. + Procedure Writers develop new, revised, or modified technical procedures which enable personnel to safety and correctly perform tasks associated with dimensional inspection, material testing, metrology, procurement, radiography, and weld inspection.

Oak Ridge, TN19 days ago

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Science Writer Jobs in the United States

Jobs

Senior Medical Writer - PublicationsSyneos Health/ inVentiv Health Commercial LLC

Technical Writer/Automotive TechnicianIconma

Infrastructure Technical WriterNeotecra, Inc.

Service WriterPotestio Brothers Equipment

Travel Nurse RN - Nurse Manager in The Lakes, NVAmbition 24Hours

Quality - Technical writerEclaro

Senior Municipal Stormwater Permit Writer (Environmental Planner 4)Department of Ecology

Senior Technical WriterHaemonetics Corporation

Science WriterAmerican Association for Cancer Research

Digital and Science Content Writer, Federal Science CommunicationsEDJ Associates,

Science WriterEssentiallySimple.net

Med Science Writer - ExemptLanceSoft Inc

Science WriterHuman Capital Resources and Concepts

Sr Med Science Writer - ExemptLanceSoft Inc

Senior Health and Science WriterAtria Physician Practice New York PC

Senior Medical WriterAmbition 24Hours Inc

Business Analyst Senior Manager, DT&IBDO USA, LLP

Senior Medical WriterArrowhead Pharmaceuticals

1099 Medical WritersPerformance Development Group

Senior Medical WriterLumanity

Clinical Evaluation Report Medical Writer (1099 Contractor)Criterion Edge Professional Services Inc.

Senior Medical Writer 28038SOMERSET STAFFING

Medical Writer - Hybrid RoleAdMed Inc.

Assistant Medical Writer - Hybrid RoleAdMed Inc.

Associate Medical Writer, In Vitro Diagnostic Regulation (IVDR) Writing ServicesCriterion Edge Professional Services Inc.

Medical WriterStaffingagencyrecruitment

Medical Writer (PhD)Medpace, Inc.

Senior Medical Writer – Medical Education / Scientific Content LeadCompose.ly

Medical Writer - Medical Communications - East CoastPrime

Senior Medical Writer (Remote)MMS

Principal Medical WriterMMS

Senior Medical Writer (Protocols)MMS

Medical WriterUpcoresolutions

Medical Writer/Content SpecialistOctane Learning

Medical Writer (Advanced Degree)Octane Learning

Technical WriterJohnson Service Group

MCTP Cyber Scenario WriterCore Government Services Corporation

Senior ICF Writer (Remote)MMS

Clin Eval Med Writer - ExemptLanceSoft Inc

Writer and Associate EditorClimate Central

Technical Writer (Quality)Sterling Engineering, Inc.

SOP WriterIntegrated Resources, Inc

Technical WriterKforce Inc.

Technical Writer / Proposal Development Intern (English Literature Major)Terrestris Global Solutions

Technical WriterGTT

Technical Writer 1Johnson Service Group

UPF Technical Procedure Writer, Level VAkima

UPF Technical Procedure Writer, Level IVAkima

UPF Technical Procedure Writer, Level IIIAkima

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