NewSenior Regulatory Medical Writer, Client-embedded, FSP Thermo Fisher ScientificSenior Regulatory Medical Writer, Client-embedded, FSPFramingham, MAStrong negotiation skills * Excellent oral and written communication skills with strong presentation skills * Significant knowledge of global, regional, national, and other document development guidelines * Great judgment and decision-making skills * Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g., Excel, Outlook). As one team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.
26808 Automotive Service Advisor/Writer Franklin Chrysler Dodge Jeep Ram26808 Automotive Service Advisor/WriterFranklin, TNFull 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. Over the years, Franklin Chrysler Dodge Jeep RAM has established a reputation for providing the greater Franklin, Tennessee area with outstanding service.
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!
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.
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.
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.
Customs Entry Writer JobotCustoms Entry WriterLong Beach, CA$26–$32 / hourThe successful candidate will be responsible for preparing, compiling and managing all documentation and records required to clear goods through the United States Customs Service (USCS), including negotiating with, and presenting declarations to, foreign and domestic customs officials. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
NewTechnical Writer / Business Analyst HTC Global Services IncTechnical Writer / Business AnalystColumbia, MOFull timeThis role involves collaborating with project teams, subject matter experts, and leadership to gather requirements, document business needs, and produce complete, compliant RFPs. Advanced proficiency in Microsoft Office, including Word, Excel, PowerPoint, and Visio, with experience using templates and style guidelines for branding consistency.
NewContent Writer Pinnacle Technical ResourcesContent WriterFort Worth, TexasContractorThe specific compensation for this position will be determined by several 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 position requires strong digital writing and editing skills, experience working within an enterprise content management system, and a portfolio demonstrating customer-facing digital content.
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.
NewSenior Technical Writer (RFP & Business Analysis) CYNET SYSTEMSSenior Technical Writer (RFP & Business Analysis)Columbia, SC$56–$61 / yearTemporaryContractorPart timeAs a nationally and locally certified Minority Business Enterprise (MBE), Cynet Systems is committed to helping organizations build high-performing teams while empowering professionals to grow rewarding careers. We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and professional staffing, powered by a high-performing recruitment engine operating across North America and Asia.
NewCustoms Entry Writer IDR, Inc.Customs Entry WriterBrentwood, TNBy submitting this application, you acknowledge and consent to engage in conversation with a recruiter or virtual recruiter from IDR Inc. and its affiliates, and contracted partners by receiving calls, AI-generated calls, texts, or emails to the contact information provided. This role is perfect for individuals with a solid background in customs entry writing or international transportation coordination, and a keen understanding of INCO terms and the Harmonized Tariff Schedule (HTS).
NewTechnical Writer Three Point Solutions, Inc.Technical WriterLos Angeles, CA$20–$22 / hourContractorCreate, edit, and maintain technical documents, manuals, work instructions, and procedures. Proofread documents for grammar, formatting, consistency, and technical accuracy.
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.
Database Report Writer Compass Health NetworkDatabase Report WriterSpringfield, MissouriRemoteFull timeYou’ll collaborate with teams across the organization to ensure accurate, timely, and actionable reporting that supports our mission to Inspire Hope and Promote Wellness—especially in rural communities where access to care matters most. This is a great opportunity for someone who enjoys working with data to solve problems, thrives in a collaborative environment, and takes pride in delivering accurate, high-quality reporting that drives impact.
NewSenior Technical Writer LeidosSenior Technical WriterVista, CA$65,650–$118,675In this role, you will partner with program managers, engineers, subject matter experts, and cross-functional teams to develop, maintain, and improve technical documentation supporting complex products, systems, and programs. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com .
NewCable Manufacturing Process Writer LeidosCable Manufacturing Process WriterHuntsville, AL$48,100–$86,950Leidos Defense Systems Sector / Manufacturing provides a diverse portfolio of systems, solutions, and services covering land, sea, air, space, and cyberspace for customers worldwide. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com .
NewA/N-SQQ-89A(V)15 Technical Writer LeidosA/N-SQQ-89A(V)15 Technical WriterChesapeake, VA$52,000–$94,000The primary function of this position is to support the development of AN/SQQ-89A(V)15 system operational and maintenance Integrated Electronic Technical Manuals (IETMs) for U.S. Navy ships in support of Program Executive Office Integrated Warfare Systems (PEO IWS 5B). If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com .
NewPBM - Proposal Strategist - Proposal Writer Southern ScriptsPBM - Proposal Strategist - Proposal WriterDallas, TXRemoteLiviniti , the leading disruptor in the PBM industry, simplifies the complexities of navigating through the Pharmacy Benefit Manager world by offering a value-added approach to ensure the employer absolute freedom, control, and choice to their health plan structure without compromising patient experiences and outcomes. The Proposal Strategist/Writer works closely with leadership throughout Liviniti to create customized responses to RFx documents that differentiates Liviniti in the market, while developing strategic content tailored to the needs of clients.
NewProcess Writer The Computer Merchant, LtdProcess WriterTallahassee, FLRemote$40–$42.50 / hourContractorWhile an hourly range is posted for this position, an eventual hourly rate is determined by a comprehensive salary analysis which considers multiple factors including but not limited to: job-related knowledge, skills and qualifications, education and experience as compared to others in the organization doing substantially similar work, if applicable, and market and business considerations. Demonstrated experience managing projects with multiple workstreams, including task decomposition, dependency tracking, and timeline management using project management tools (e.g., MS Project, Planner, or equivalent).
Senior Medical Writer/Principal Medical Writer - Regulatory Writing Thermo Fisher ScientificSenior Medical Writer/Principal Medical Writer - Regulatory WritingMorrisville, North CarolinaThe 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. 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.
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.
Medical Writer Disc Medicine IncMedical WriterMassachusetts, MA$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.
NewPrincipal Medical Writer - Publications Syneos HealthPrincipal Medical Writer - PublicationsPennsylvaniaInteracts and builds good working relationships with clients, department head, and team members 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.
NewSenior Medical Writer - FSP ParexelSenior Medical Writer - FSPNorth CarolinaServe as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
NewSr Medical Writer - Late Phase - Inflammation Syneos HealthSr Medical Writer - Late Phase - InflammationNorth CarolinaInteracts 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.
Sr. / 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.
Sr. 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.
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.
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.
Senior Medical Writer, Medical Communications Precision Medicine Group LLCSenior Medical Writer, Medical CommunicationsNew York, NY$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.
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.
NewSenior Medical Writer - FSP Parexel International CorpSenior Medical Writer - FSPNCServe as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
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.
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.
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.
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.
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.
Senior Medical Writer BioMarin Pharmaceutical IncSenior Medical WriterCAFilling this need with a regular full-time employee will enable BioMarin to reduce writing-related CRO and contractor costs, increase Global Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications.
Medical 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.
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.
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.
Medical 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.
Sr. 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 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.
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.
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.