NewTechnical Writer CredenceTechnical WriterRobins Air Force Base, GAApply writing skills and substantial knowledge of basic principles and specialized vocabulary of appropriate subject-matter fields to accurately communicate scientific and technological developments to expert and other interested audiences. The Air Force Distributed Common Ground System (AF DCGS) is an intelligence enterprise system, comprised of active duty, Air National Guard (ANG), and mission partner sites, interconnected by a robust communications infrastructure spanning the globe.
NewQuality - Technical writer ECLAROQuality - Technical writerNew Brunswick, NJ$42.85–$45.45 / hourResponsibilities: 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.
NewTechnical Investigation Writer JouléTechnical Investigation WriterBridgewater Township, NJRemote$40 / hourPartner with Technical Services, Engineering and Manufacturing team members to determine the scope, impact and risk associated with the deviations/non-conformances observed in Manufacturing and Packaging department. Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the reported deviation using Kepner-Tregoe, Ishikawa, Fish bone, 5 Why methods.
Senior Scientific Writer - CBM Lab Shirley Ryan AbilityLabSenior Scientific Writer - CBM LabChicago, IllinoisThe Senior Scientific Writer will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contributing to the team efforts and showing respect and compassion for patients and their families, fellow employees, and all others with whom there is contact at or in the interest of the institute. Keep project teams informed of institutional changes within SRAlab as well as changes within the federal funding structure that affect the execution of the existing projects or potential renewal of funding.
Scientific Writer - Integrative Oncology City of HopeScientific Writer - Integrative OncologyIrvine, CAYou will be responsible for producing high-quality, scientifically accurate, and engaging written content focused on Integrative Oncology, which combines mind-body practices, natural products, and lifestyle modifications with conventional treatments to support the Cherng Centers research, clinical, and educational initiatives. As a successful candidate, you will: • Write, edit, content style, and grammar/spelling, and proofread R01 and R01-like grant proposals, scientific manuscripts, for peer review, clinical study protocols, or other scientific documents for faculty research fellows and students.
NewScientific Writer - Orange County City of HopeScientific Writer - Orange CountyIrvine, CAAs a successful candidate, you will: Write, edit (content, style and grammar/spelling), and proofread¬ R01 and R01-like grant proposals, scientific manuscripts for peer review, INDs, clinical and IRB protocols, or other scientific documents for faculty, research fellows, and students. Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
Scientific Writer - Translational Development RD PartnersScientific Writer - Translational DevelopmentMadison, New Jersey£113,102–£141,396Ensure timely delivery for the TD writing book of work such as pre-clinical reports, and Translational biomarker reports across areas of focus (eg, multiple myeloma, lymphoma, myeloid, erythroid disorders). Collaborate with TD scientists and representatives of other functions (eg, Clinical, Non-Clinical Development, Pharmacology, Drug Metabolism & Pharmacokinetics) as needed to execute publications/reports/regulatory documents.
Nonclinical Regulatory Document and Scientific Writer Artech LLCNonclinical Regulatory Document and Scientific WriterGiralda Farms, NJ$64–$68.45 / hourReporting to the Program Management Lead, the incumbent will be part of the late development translational group based in Giralda Farms NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, translational portions of clinical/pharmacology summaries, briefing books, CSRs, investigator brochures) in conjunction with Translational scientists. " Strong verbal and written communication skills with experience in developing written documents such as primary manuscripts/publications/reviews, disease strategies, mechanism slides, regulatory submissions, strategic communications, literature/market/pt segment analyses.
Scientific Writer (Onsite Consultant) NanobiosymScientific Writer (Onsite Consultant)Cambridge, MAThe ideal candidate will have a PhD or Master's degree in a science discipline, and prior experience as a senior editor or lead writer for leading scientific journals, magazines, or research institutions is preferred. This is an onsite consulting role requiring close collaboration with scientists, researchers, and leadership teams to translate complex scientific concepts into high-impact written content for diverse audiences.
Scientific Writer, Integrated Research Management Revolution Medicines IncScientific Writer, Integrated Research ManagementRedwood City, CA$143,000–$178,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The role partners closely with nonclinical subject matter experts (SMEs) in pharmacology, toxicology, and DMPK, as well as Regulatory Affairs, Regulatory Operations, and Medical Writers, to ensure nonclinical strategy and content are scientifically rigorous, aligned, and submission-ready.
Scientific Writer, Integrated Research Management Revolution MedicinesScientific Writer, Integrated Research ManagementRedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The role partners closely with nonclinical subject matter experts (SMEs) in pharmacology, toxicology, and DMPK, as well as Regulatory Affairs, Regulatory Operations, and Medical Writers, to ensure nonclinical strategy and content are scientifically rigorous, aligned, and submission-ready.
Scientific Writer Houston Methodist HospitalScientific WriterHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to the preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation.
Expert Scientific Writer Novartis AGExpert Scientific WriterEast Hanover, NJReady to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureBenefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally. Support publication strategy, cross-functional projects, problem-solving, documentation, archiving, and work across multiple therapeutic areas and brands.
Senior Scientific Writer - Urology - Kobashi HMRISenior Scientific Writer - Urology - KobashiTexasThis role must also have familiarity with scientific and clinical research and will conduct comprehensive literature searches for writing and editing abstracts, manuscripts, review articles, grant applications, clinical study protocols, investigator brochures, consent forms, presentations and progress reports for both scientific and lay audiences. QUALITY/SAFETY ESSENTIAL FUNCTIONS Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to the preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation.
Scientific Writer HMRIScientific WriterTexasSERVICE ESSENTIAL FUNCTIONS Facilitates writing, editing, and preparation of high quality written scientific documents for grant applications, publications, scientific manuscripts for peer review, white papers, protocols, and other scientific or administrative reports. The health system consists of eight hospitals: Houston Methodist Hospital, its flagship academic hospital in the Texas Medical Center, seven community hospitals and one long-term acute care hospital throughout the Greater Houston metropolitan area.
Scientific Writer/Editor - ON-CALL ICF International IncScientific Writer/Editor - ON-CALLCA$61,232–$104,094 / yearPay Range - There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future.
Scientific Writer/Editor - ON-CALL ICFScientific Writer/Editor - ON-CALLPay Range - There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future.
Senior Scientific Writer - Otolaryngology HMRISenior Scientific Writer - OtolaryngologyTexasQUALITY/SAFETY ESSENTIAL FUNCTIONS Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to the preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation. The health system consists of eight hospitals: Houston Methodist Hospital, its flagship academic hospital in the Texas Medical Center, seven community hospitals and one long-term acute care hospital throughout the Greater Houston metropolitan area.
Scientific Writer and Research Analyst (Posting Title) American Association for Cancer ResearchScientific Writer and Research Analyst (Posting Title)Philadelphia, PennsylvaniaFull timeIn this role, the candidate will contribute to the preparation of high-impact scientific documents—such as cancer progress reports, white papers, and scholarly articles—that highlight advances in blood cancer and communicate their significance to diverse audiences, including basic and clinical scientists, clinicians, policymakers, patient advocates, and the public. Overview: We are seeking a highly skilled and motivated Scientific Research Analyst with deep expertise in one or more major subtypes of blood cancer and other related syndromes (leukemia, lymphoma, multiple myeloma, MDS, CHIP).
Scientific Writer / Project Development Scientist City of HopeScientific Writer / Project Development ScientistDuarte, CAThis is a unique hard-money position, where Dr. Erhunmwunsee seeks a research protégé who wishes to learn and grow under her mentorship the ideal candidate will advance in their career as the Lung, Justice, & Equity (LJE) lab and the Health Access and Community Enrichment office grows and succeeds. Lead end-to-end grant and scientific writing efforts, including identifying funding opportunities, developing and submitting proposals, managing deliverables, and representing the research program through publications, presentations, and external collaborations.
NewTechnical Writer - Scientific - II Integrated Resources, IncTechnical Writer - Scientific - IIRaynham, MassachusettsContractorJob DescriptionTechnical and Scientific ReviewerSummary:The Technical and Scientific Reviewer provides leadership, motivation, and strategic direction for the scientific and technical content for prepared regulatory documents by the Medical Operations Team. Technical Writer - Scientific - IIA 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.
NewTechnical Writer - Scientific-II Integrated Resources, IncTechnical Writer - Scientific-IISomerville, New JerseyContractorThe candidate will be an experienced professional with a focus on creating forms, templates, data entry and organizing files in structured folders and SharePoint sites. The successful candidate will contribute to dictionary of terms for understanding the hierarchy of products, disease states and specialties to build the smart search tools.
Contract Medical Writer (Scientific Communications) MJH Life SciencesContract Medical Writer (Scientific Communications)RemoteThis role partners with Medical Affairs and account teams to create advisory board content, training resources, and scientific messaging that supports healthcare professionals across live, digital, and field-facing channels. We are seeking a Contract Medical Writer (Scientific Communications) to support the development of high-quality, evidence-based medical communications materials.
Scientific/Medical Writer MyOmeScientific/Medical WriterBoston, MARemote$100,000–$140,000 / yearWe combine clinical-grade whole genome sequencing, advanced AI methods for genome interpretation, and seamless digital tools for doctors and patients to order and access results. An early-stage biotechnology/genetics firm is seeking a full-time Scientific/Medical Writer to research, write, and edit the company's scientific reports.
Scientific Technical Writer/Editor BLN24Scientific Technical Writer/EditorMcLean, VAFull timeWorking closely with NOAA leadership, researchers, scientists, program managers, and stakeholders, the ideal candidate combines exceptional writing and editing skills, scientific literacy, and strategic communications expertise to communicate NOAA's research outcomes to policymakers, Congress, the weather enterprise, and the public. Bachelor's degree in Journalism, Communications, English, Science Communication, Atmospheric Science, Environmental Science, Meteorology, Public Policy, or related discipline, Minimum six (6) years of professional experience in technical writing, scientific communications, journalism, public affairs, or strategic communications.
NewMedical Writer - Scientific Communications Perspective TherapeuticsMedical Writer - Scientific CommunicationsUnited StatesFull timeProject Support: Provide medical writing support across various stages of clinical development, including early-phase studies, late-stage clinical trials, and nonclinical and CMC teams as needed. Cross-Functional Collaboration: Work closely with clinical development, regulatory affairs, and other stakeholders (e.g., nonclinical, CMC etc) to ensure that all medical writing deliverables meet project objectives, timelines, and internal and external requirements.
NewMedical Writer, Scientific Intelligence Vaniam GroupMedical Writer, Scientific IntelligenceRemoteA Day in the Life Deliverables Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials. Actively contribute to the ongoing improvement of Vaniam Group’s LLM by applying and sharing deep scientific and therapeutic area expertise to inform, validate, and refine AI outputs.
Scientific Digital Content Writer (SEO & AI-Optimized Content) Thermo Fisher Scientific IncScientific Digital Content Writer (SEO & AI-Optimized Content)Pleasanton, CA$75,000–$110,000 / yearWe provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.
Scientific Technical Writer Medpace, Inc.Scientific Technical WriterCincinnati, OhioQualifications: 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.
Scientific Technical Writer/Editor (52008) Gap Solutions, Inc.Scientific Technical Writer/Editor (52008)Bethesda, MDThe Scientific Technical Writer/Editor shall provide comprehensive editorial, writing, research, and multimedia support services to support FIC communications. Services shall include content development, editorial planning, production coordination, and dissemination support across newsletters, websites, and social media platforms.
Senior Scientific Associate / Senior Medical Writer - Promotional Medical Writing (CST) Precision AQSenior Scientific Associate / Senior Medical Writer - Promotional Medical Writing (CST)RemoteAs a Senior Scientific Associate , you will write medical content for our clients working with internal teams to ensure that the client vision is achieved impacting our clients who are developing groundbreaking medicines/treatments who are working to make medicines accessible and affordable. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Scientific Content Writer - Marketing Omega Bio-tek, Inc.Scientific Content Writer - MarketingNorcross, GAFull timeDescription: Research, develop, write, and edit technical and informational materials for various Marketing and company needs in one or more of the following areas: marketing collateral (internal and front facing), application sheets, customer bulletins and white papers, or other electronic documentation for products and/or other miscellaneous publications, both for internal and external customer usage. Ability to work collaboratively, meet deadlines, have attention to details, perform multiple tasks simultaneously and prioritize.
Medical Content Writer Ova TechnologiesMedical Content WriterAlpharetta, GARemoteJoin our growing healthcare content team as a Medical Content Writer , where you will create accurate, engaging, and evidence-based medical content for healthcare professionals, patients, pharmaceutical companies, and digital healthcare platforms. The ideal candidate possesses excellent writing skills, a strong understanding of medical terminology, and the ability to translate complex scientific concepts into clear, reader-friendly content.
Oncology Scientific Lead, Med Com (Associate Scientific Dir) IREOncology Scientific Lead, Med Com (Associate Scientific Dir)Raleigh, North CarolinaRemoteDemonstrable history of relevant high-level writing support and review (e.g, while at a medical communications agency), including proficiency with ICMJE and GPP guidelines; reviewing and interpreting scientific and technical journal content; knowledge of diverse prescribed styles and formats. This role encompasses high-level writing, peer-review of project deliverables, strategic support and client engagement as determined by the respective aligned account leaders.
NewProgram Manager, Scientific Outreach and Communications University of Massachusetts Medical SchoolProgram Manager, Scientific Outreach and CommunicationsWorcester, MassachusettsThis role is responsible for coordinating STEM programming for the Worcester Public School (WPS) District and supporting faculty and trainees in the development of scientific materials, including fellowship and training grant applications. Collaborate with scientific writers, faculty, and trainees to support preparation of fellowship applications, including: Edit application components (e.g., research statements, training plans, personal statements).
Program Manager, Scientific Outreach and Communications (2026-49873) University of MassachusettsProgram Manager, Scientific Outreach and Communications (2026-49873)Worcester, MAAll Academic Accounting & Finance Administrative Professional Administrative Support Advancement Basic Science Biotechnology Clinical Research Environmental Health & Safety Executive Faculty Healthcare Human Resources Information Technology Interns Library Maintenance and Facilities Management Nursing Office Assistant Other Post Doc Professional Technician I Public Safety Research Residents Retail & Dining Services Staff Assistant Staff Associate Volunteer. All Bedford Boston Brockton Brockton Canton Charlestown Danvers Devens Fall River Fitchburg Holyoke Jamaica Plain Jamaica Plan Lincoln Mattapan North Hampton North Quincy Pocasset Shrewsbury Springfield Taunton Tewksbury Waltham Westborough Westfield Woburn Worcester Wrentham.
Senior Director, Global Scientific and Regulatory Documentation, Content Strategy Bristol-Myers Squibb CoSenior Director, Global Scientific and Regulatory Documentation, Content StrategyPrinceton, NJ$224,940–$272,579 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Science Writer Dana-Farber Cancer Institute IncScience WriterBOSTON, MARemote$80,100–$103,200 / yearHe/she will work with the Senior VP of Communications, the directors of Editorial and Creative Services and Media Relations, as well as other Communications Department staff and DFCI senior administrators, to formulate and produce articles and publicity materials that promote understanding and support for Dana-Farber's research and clinical mission. Write, ghost write, and edit materials for a wide array of non-publication projects, including letters, memos, scientific symposia, research seminars, organizational changes within DF/HCC, trends in research and care.
Program Manager, Scientific Outreach and Communications UMass Chan Medical SchoolProgram Manager, Scientific Outreach and CommunicationsWorcester, MAThis role is responsible for coordinating STEM programming for the Worcester Public School (WPS) District and supporting faculty and trainees in the development of scientific materials, including fellowship and training grant applications. Collaborate with scientific writers, faculty, and trainees to support preparation of fellowship applications, including: Edit application components (e.g., research statements, training plans, personal statements).
NewDirector, Scientific Writing AstraZeneca PlcDirector, Scientific WritingGaithersburg, MD$164,981–$210,651 / yearPersonally author and provide oversight of scientific writing outputs (abstracts, posters, manuscripts, study reports, protocols, HTA dossier summaries) for real-world evidence and observational studies conducted by the Oncology Outcomes Research team, including database studies, registry analyses, and chart reviews. Director, Scientific Writing reports to the Head, CODE and will be leading and running a high-performing scientific writing function, overseeing a blended team of internal writers and contractors to deliver high-quality outputs across interventional trials and real-world/observational studies.
NewScientific Project Director Cancer Neuroscience University of Texas MD Anderson Cancer CenterScientific Project Director Cancer NeuroscienceHouston, TXPreferred: Demonstrates ability to manage a portfolio of complex, research-driven projects including execution, tracking, and reporting of funded initiatives; has strong scientific literacy with the ability to read and interpret scientific and clinical proposals, understand research methods, milestones, and risks, and proactively assess project progress; communicates effectively with multiple principal investigators and stakeholders; is highly organized, solutions-oriented, and innovative with the ability to independently identify opportunities and propose strategies; exhibits strong written and verbal communication skills; and has experience with budgets and philanthropy or donor-funded projects as a plus. Develops and maintains a systematic ROI tracking framework for all CNP-funded projects capturing metrics such as publications, subsequent grant funding, intellectual property disclosures, patent application filings, clinical translation milestones, and philanthropic leverage attributable to CNP investment; produces regular ROI reports for program leadership and philanthropic stakeholders, and continues monitoring return on investment for a defined period following project close.
Scientific Lead - Medical Communications ICON PlcScientific Lead - Medical CommunicationsBlue Bell, PABased on this and the overall description, the SL role will fall broadly across the following approximate allocations (individual client account teams may have, from time to time, specific needs that may alter these allocations: Primary responsibilities for this role comprise content oversight and quality control including but not limited to: reviewing of assigned writers' work. Demonstrable history of relevant high-level writing support and review (e.g, while at a medical communications agency), including proficiency with ICMJE and GPP guidelines; reviewing and interpreting scientific and technical journal content; knowledge of diverse prescribed styles and formats.
Principal Medical Writer MJH Life SciencesPrincipal Medical WriterRemoteYou actively use tools such as ChatGPT, Claude, or AI-assisted research and writing platforms to improve how you work and can clearly articulate how they enhance output quality and efficiency — while maintaining scientific integrity and compliance. Provide mentorship, training, and editorial guidance to junior Medical Writers and Editors, supporting their development and helping the team consistently deliver high-quality work.
Technical Writer / Communications Specialist (On-Site) Oxley Enterprises®, Inc.Technical Writer / Communications Specialist (On-Site)Silver Spring, MD$87,103–$97,997 / yearFull timePosition Description: The Technical Writer / Communications Specialist provides professional writing, editing, documentation, and outreach support for Joint Pathology Center(JPC) research, education, and public engagement activities. Oxley Enterprises®, Inc. is a certified service-disabled veteran-owned (SDVOSB), veteran-owned (VOSB), and woman-owned small business (WOSB) that has 26 years of experience building and delivering quality IT systems and programs.
Associate Scientific Director, Medical Communications Precision AQAssociate Scientific Director, Medical CommunicationsThis compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
Medical Writer Disc Medicine IncMedical WriterMA$117,000–$143,000 / yearCommunicate and coordinate with line-function team members to gather, organize, and compile information towards the development and planning of writing scientific, clinical, and regulatory documents; communicate deliverables needed, writing process and timelines, and hold team members accountable to agreed-upon dates for deliverables. RESPONSIBILITIES: Partner and collaborate with clinical and regulatory team members in the preparation of clinical protocols and regulatory documents; participate in study results interpretations and manage the document review/approval process to capture comments and resolve conflicts, including running round-table meetings.
Associate Medical Writer MJH Life SciencesAssociate Medical WriterCranbury, New JerseyThe Associate Medical Writer at Pharmacy Times Continuing Education (PTCE) plays a vital role in supporting the Scientific Affairs and Business Development teams by contributing to the development of CE-certified educational content. Ability to interpret complex clinical data and outcomes reports to identify learning trends and educational needs.
Medical Writer MJH Life SciencesMedical WriterRemoteIn this role, you’ll translate complex clinical data into clear, compelling deliverables across multiple formats, such as articles, white papers, slide decks, digital media, and live event content. The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific content for a variety of audiences, including healthcare professionals, patients, and industry stakeholders.
NewTechnical Writer ATCCTechnical WriterManassas, Virginia$68,000–$75,000 / yearFull timeWorking in a science-focused environment, the Technical Writer helps create consistent, accurate, and compliant documentation, reviews scientific literature and data, and supports website content and document accessibility initiatives. This onsite position in Manassas, VA supports ATCC Federal Solutions by researching, organizing, writing, reviewing, and editing scientific and technical information for use in documentation across multiple platforms.
Technical Writer/Editor III General AtomicsTechnical Writer/Editor IIISan Diego, CAMust possess: The ability to develop, acquire, interpret and communicate engineering/scientific technical data; The ability to develop and communicate new concepts and apply them accurately throughout an evolving environment; The ability to maintain the confidentiality of sensitive information; The ability to organize, schedule and coordinate work phases and determine the appropriate approach at the task or project level; Leadership and organization skills in order to work with management and customers and represent the organization; and, The ability to identify issues and develop advanced solutions to a variety of complex technical and administrative problems. Under general supervision, this position participates with management and engineering/scientific teams to establish objectives, plans, and timelines for the development of comprehensive technical documents such as procedure manuals, operational specifications, training manuals, presentations, articles and related technical publications.