NewDigital Health / Medical Devices Proposal Manager (RFP Writer) - # 26-17509 US Tech Solutions, Inc.Digital Health / Medical Devices Proposal Manager (RFP Writer) - # 26-17509Dallas, TXThis individual will lead the end-to-end proposal development process, partnering with cross-functional teams to deliver high-quality, compliant, and compelling responses to RFPs, RFIs, and other customer requests. The ideal candidate is a strategic writer with strong healthcare industry knowledge, exceptional project management skills, and a proven ability to manage multiple proposal efforts while meeting aggressive deadlines.
45572 Automotive Service Advisor/Writer - Express Lane Jacksonville Chrysler Jeep Dodge Ram of Arlington45572 Automotive Service Advisor/Writer - Express LaneJacksonville, FLFull timeExpress Lane Service Advisor Jacksonville Chrysler Jeep Dodge Ram Arlington is looking for an Express Service Advisor to join their team! Experience in a Express Lane Advisor or Service Advisor role strongly preferred.
Automotive Service Advisor/Writer Napleton Northlake Chrysler Dodge Jeep RamAutomotive Service Advisor/WriterLake Park, FLFull timeThey greet and consult customers on service needs, perform a thorough vehicle walk around inspection as part of the write-up, sell and up sell services by emphasizing value, keep customers updated on services, field all live service calls, and take ownership of the customer’s experience by carrying out those additional assignments that allow the dealership to leave an impressionable experience with the customer. As a Service Advisor, you will be experienced and aware of the latest customer service practices and be a persistent problem solver.
45478 Automotive Service Advisor/Writer Gillman Chrysler Jeep Dodge Ram45478 Automotive Service Advisor/WriterHouston, TXFull timeGillman Chrysler Jeep Dodge Ram in Houston is looking for experienced Service Advisors to join their industry leading service team. Service Advisors remain involved with the delivery of the vehicle to the customer upon completion to ensure all customer concerns can be addressed.
68732 Automotive Service Advisor / Service Writer CareerBuilder-Stellantis68732 Automotive Service Advisor / Service WriterAlexandria, LAFull timeService Advisor Walker Chrysler Dodge Jeep Ram in Alexandria is looking for experienced Service Advisors to join their industry leading service team! Set and manage the expectations of the service delivery for both the customers and mechanics.
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.
Technical Writer - Intermediate Pinnacle Technical ResourcesTechnical Writer - IntermediateHouston,, Texas$30–$35 / hourContractorThe specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. This role requires excellent communication skills, a strong understanding of technical concepts, and the ability to translate complex information into clear and concise documentation.
UX Writer Pinnacle Technical ResourcesUX WriterCulver City,, California$70–$75 / hourContractorThe specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. Successfully placed or hired candidates would only be asked for banking details after accepting an offer from us during our official onboarding processes as part of payroll setup.
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.
Dodge Service Writer Hendrick Automotive Group CorporateDodge Service WriterCary, North CarolinaFull timeWork includes inspection of customer vehicles and frequent movement around the Service Department to convey information between customers and service technicians. Frequently interacts with customers, service manager and service technicians, and employees from various departments in the dealerships.
Auto Care Center Service Writer WalmartAuto Care Center Service WriterNew Bloomfield, MO$15–$28These Auto Care Center roles focus on the needs of our customers who entrust us with the care of their vehicles as they shop for merchandise and services offered at Walmart. Programs range from high school completion to bachelor's degrees, including English Language Learning and short-form certificates.
Senior Director, Product Strategy & GTM Offers - Fuelman CorpaySenior Director, Product Strategy & GTM Offers - FuelmanAtlanta, GAThe Senior Director, Product Strategy & GTM Offers will serve as the commercial strategy owner for Fuelman, translating market intelligence, customer needs, competitive dynamics, and product capabilities into clear offers, sharper messaging, stronger sales narratives, and better business outcomes. Building and maintaining rigorous competitive intelligence system … tracking competitor pricing, rebates, fees, network claims, product capabilities, value propositions, customer segments, sales motions, and marketing messages.
45286 Automotive Service Advisor/Writer Lithia Chrysler Dodge Jeep Ram Of Corpus Christi45286 Automotive Service Advisor/WriterCorpus Christi, TXFull timeThey greet and consult customers on service needs, perform a thorough vehicle walk around inspection as part of the write-up, sell and up sell services by emphasizing value, keep customers updated on services, field all live service calls, and take ownership of the customers experience by carrying out those additional assignments that allow the dealership to leave an impressionable experience with the customer. Lithia Chrysler Jeep Dodge of Corpus Christi is looking to add motivated Automotive Service Advisors to their dynamic team!
Grant Writer-Lead J-U-B ENGINEERS, IncGrant Writer-LeadKennewick, WA$82,000–$89,000 / yearFull timeWe are looking for a collaborative and solutions-oriented Grant Writer-Lead/Funding Specialist to serve within a multidisciplinary team, you will prepare comprehensive funding plans, federal and state grant applications, and technical reports. You will be the bridge between our clients' needs and the complex requirements of funding agencies, researching opportunities and managing the lifecycle of successful grants.
NewSenior Medical Writer/Principal Medical Writer - Regulatory Writing Thermo Fisher Scientific IncSenior Medical Writer/Principal Medical Writer - Regulatory WritingMorrisville, NCThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. What You'll Do: Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
Multispecialty Medical Writer, Accredited Medical Education MJH Life SciencesMultispecialty Medical Writer, Accredited Medical EducationRemoteWrite and edit across multiple deliverables, including peer-reviewed publications, trade journal articles, monographs, slide decks, scripts, and digital programs. This role involves translating complex scientific and clinical information into clear, engaging content while ensuring accuracy, regulatory compliance, and alignment with relevant professional society (e.g.
Senior Medical Writer - Medical Information Thermo Fisher Scientific IncSenior Medical Writer - Medical InformationWilmington, NCThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. Develop complex medical and scientific documents, including AMCP dossiers, infographics, slide presentations, manuscripts, study documents for complex programs.
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.
Principal Medical Writer, Cardio/Metabolic Health ProPharma Group Holdings LLCPrincipal Medical Writer, Cardio/Metabolic HealthChicago, ILWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Associate Director, Regulatory and Medical Writer Ionis Pharmaceuticals IncAssociate Director, Regulatory and Medical WriterCarlsbad, CARemote$142,588–$201,472 / yearRESPONSIBILITIES: Working with the Executive Director, Regulatory and Medical Writing, lead the development, authoring, and delivery of complex regulatory documents such as clinical study reports and marketing application summary documents (Module 2), and lead and/or contribute to Investigator's Brochures, clinical study protocols, and briefing documents. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
Sr Medical Writer Publications - Sponsor Dedicated - Remote Based Syneos HealthSr Medical Writer Publications - Sponsor Dedicated - Remote BasedPennsylvaniaRemoteInteracts 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. 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.
NewSr. Medical Writer (Regulatory) Syneos HealthSr. Medical Writer (Regulatory)MarylandInteracts 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. • 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.
NewSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK Syneos HealthSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UKIndianaInteracts 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. • 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.
Senior Medical Writer ProPharma Group Holdings LLCSenior Medical WriterChicago, ILWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Medical Writer, Accredited Medical Education MJH Healthcare Holdings LLCMedical Writer, Accredited Medical EducationNYRemote$85,000–$95,000 / yearWrite and edit across multiple deliverables, including peer-reviewed publications, trade journal articles, monographs, slide decks, scripts, and digital programs. This role involves translating complex scientific and clinical information into clear, engaging content while ensuring accuracy, regulatory compliance, and alignment with relevant professional society (e.g.
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.
Senior Medical Writer BioMarin Pharmaceutical IncSenior Medical WriterCA$142,100–$195,360 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
Freelance Medical Writer Hueman PE Talent SolutionsFreelance Medical WriterBelmont, MAAt CLD, we support our customers in developing customized training for their commercial sales teams, medical teams (MSLs), patients, and physicians. This role requires the ability to independently research primary literature, apply sound analytical judgment, and synthesize findings into well-organized, detail-oriented deliverables under tight deadlines.
Medical Writer - Hybrid Role AdMed Inc.Medical Writer - Hybrid RolePhiladelphia, PAAdMed 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.
Principal Medical Writer IREPrincipal Medical WriterAs a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development.
Medical Writer PerceptiveMedical WriterThe Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review charters, clinical data forms, manual case report forms, applicable reviewer training materials, project deviations and supplementary imaging reports, using available central content and templates. Serve as the medical writing representative on assigned project teams communicate content requirements, Coordinate and conduct interdepartmental team reviews of draft and final documents, Evaluate progress on tasks, identify issues and facilitate resolutions, and advance document development to approval, according to Calyx and/or client guidelines/SOPs.
Senior Medical Writer, Medical Communications Precision Medicine Group LLCSenior Medical Writer, Medical CommunicationsNY$95,000–$125,000 / yearThis 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.
Senior Regulatory Medical Writer Ionis Pharmaceuticals IncSenior Regulatory Medical WriterCarlsbad, CARemote$113,000–$142,426 / yearThis role includes responsibilities throughout the lifecycle of a document including working cross-functionally to interpret source information (including leading data interpretation meetings), leading key messaging meetings, writing content following US and international regulations (including Marketing Application Module 2 summary documents), conducting quality control (QC) reviews, resolving Quality Assurance (QA) audit findings, and working with Regulatory Operations for publishing and submission. Experience writing, as lead and/or contributor, important regulatory and clinical documents such as clinical study reports (all sections including safety narratives), Investigator's Brochures, clinical study protocols, drug marketing application summary documents, Investigational New Drug applications, clinical sections of New Drug Applications, and other regulatory documents (e.g., Briefing Documents) for submission.
Senior Medical Writer (Oncology) MJH Life SciencesSenior Medical Writer (Oncology)RemotePosition Overview: As a Senior Medical Writer in the Clinical Communications team, you will be a pivotal player in crafting high-quality, scientifically accurate content aimed at educating oncology care providers. Ensure the scientific and clinical accuracy of all content through a global fact-check of referenced literature and appropriate annotation following AMA style (11th edition) and in-house guidelines.
Contract Medical Writer (Publications & Congress Support) MJH Life SciencesContract Medical Writer (Publications & Congress Support)RemoteWe are seeking a Contract Medical Writer (Publications & Congress Support) to develop high-quality, scientifically rigorous content for peer-reviewed publications and congress-related deliverables. This role partners with Medical Affairs teams, investigators, and KOLs to translate complex clinical and scientific data into clear, evidence-based communications for global scientific audiences.
Senior Medical Writer LumanitySenior Medical WriterYardley, PennsylvaniaRemoteResponsibilities / 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.
NewMedical Writer - I Integrated Resources, IncMedical Writer - IRaynham, MassachusettsContractormedical 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 experienceKnowledge/RequirementsExcellent English language skills, especially writing and proofreading. Job DescriptionOverview: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 Client Strategic Medical Affairs Team for a wide range of audiences.
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.
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.
Medical Writer BioMarin Pharmaceutical IncMedical WriterSan Rafael, CA$74,100–$100,000 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
NewMedical Writer Integrated Resources, IncMedical WriterRaynham, MassachusettsContractorJob DescriptionPosition 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. 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.
NewSr. Medical Writer Integrated Resources, IncSr. Medical WriterMansfield, MassachusettsFull timeThis position will meet and communicate regularly with Clinical Affairs, PACE, R&D, marketing, Sales, KOL's and others as necessary to build and collaborateQualificationsSpecial Notes:100% remote work is possible, on site is preferredPHD with 5+ years of experience or Nurses with 10+ years of experience is requiredThe Medical Writer has to review the post market surveillance data, has to create a demonstration of safety reportsExtensive experience with Clinical Evaluation Report is required, person has to be able analyze complex scientific informationPost Marker Surveillance experience is requiredGood understanding of risk management and hands on experience with risk management documentation is requiredAdditional InformationKind Regards,Sabanaaz ShaikhClinical RecruiterIntegrated Resources, Inc. abstracts, manuscripts, presentationsRequires a strategic understanding of the therapeutic areas, business and study objectives as well as statistical dataIndependently, critically writes and edits scientifically complex documents for substantial intellectual contentReviews and provides input on the data being considered for publication to ensure alignment with current medical issues and corporate goalsExpert knowledge of clinical research, device/drug development processes, regulatory requirements, and good clinical practicesAbility to understand and interpret statistical results of clinical studies; ability to summarize complex results and present them in a clear, concise, and scientifically accurate manner to a wide range of audiencesNon-essential functions:1.
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.
Medical Writer / Medical Reviewer Consultant - Oncology Ovarian Cancer ClinChoice IncMedical Writer / Medical Reviewer Consultant - Oncology Ovarian CancerCARemoteThe successful candidate will collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, Biostatistics, and external experts to ensure scientific accuracy, compliance, and timely execution of deliverables. We are seeking an experienced Medical Writer or Medical Reviewer with expertise in Ovarian Cancer and Gynecologic Oncology to support the development, review, and delivery of high-quality scientific and medical content.
Medical Writer SystImmune, Inc.Medical WriterPrinceton, NJ$80,000–$130,000 / yearThe 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.
Medical Writer BGBxMedical Writer$70,000–$95,000 / yearOur current staff is represented by a wide range of higher learning institutions, including (but not limited to) Albert Einstein, Carnegie Mellon, Columbia, Cornell, Duke, Harvard, Johns Hopkins, New York University, Northwestern, Memorial Sloan Kettering, Mt. Sinai, Princeton, Rockefeller, Rutgers, Stanford, Thomas Jefferson, UC Berkeley, UC San Francisco, University of Chicago, University of Maryland, University of Massachusetts, University of Pittsburgh, University of Pennsylvania, University of the Sciences (Philadelphia), and Yale.
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 - Clinical Regulatory Documentation Perspective TherapeuticsMedical Writer - Clinical Regulatory DocumentationUnited StatesFull timeReporting to the Head of Medical/Regulatory Writing, the Medical Writer – Clinical Regulatory Documentation will be responsible for the preparation and delivery of high-quality, scientifically accurate, and regulatory-compliant clinical/medical documentation to support clinical development and regulatory submissions. Project Support: Provide medical writing support across various stages of clinical development, including early-phase studies, late-stage clinical trials, and regulatory submissions.
Senior Medical Writer OSI PharmaceuticalsSenior Medical WriterBoulder, ColoradoWorks with clinical, data management and biostatistics staff to develop report formats and write final drafts of clinical study reports. May draft manuscripts, Investigator’s brochures, Annual Reports, Protocols and package insert materials or promotional materials, as needed by individual project teams in Clinical Development.