Medical Writer II/ Marketing Healthcare Writer Integrated Resources, IncMedical Writer II/ Marketing Healthcare WriterMorristown, NJRemote$60–$66 / hourKey Responsibilities: Collaborate with marketing teams to develop and refine digital copy for websites, email campaigns, social media, and other promotional channels. Manager Notes: Team size: 8 people, Digital marketing, establish products, supporting marketing efforts for over 30 brand products .
NewMedical Writer, Medical Communications Precision Medicine Group LLCMedical Writer, Medical CommunicationsNY$80,000–$110,000 / yearIndividuals without prior medical writing experience will build core competencies in medical writing, communication, and project collaboration through structured guidance, feedback, and progressive responsibility, while medical writers with prior experience will operate with greater independence. 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 - Promotional Medical Writing Precision Medicine Group LLCSenior Medical Writer - Promotional Medical WritingNYRemote$75,000–$112,500 / 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 - Perlmutter Cancer Center Clinical Trials Office New York University School of MedicineMedical Writer - Perlmutter Cancer Center Clinical Trials OfficeNew York, NY$84,577.92–$88,200 / yearThe Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.
USA-Medical Writer II (Clinical) MindlanceUSA-Medical Writer II (Clinical)Morristown, NJRemoteDigital marketing, establish products, supporting marketing efforts for over 30 brand products " Possibly of extension ***Manager strongly prefers candidates in EST time zone*** " 40 hours depending on business needs " 100% remote, must work est hours. Collaborate with marketing teams to develop and refine digital copy for websites, email campaigns, social media, and other promotional channels.
Medical Writer / Clinical Document - Remote YO AI LabsMedical Writer / Clinical Document - RemoteNew York, NYRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Medical Writer - Remote YO AI LabsMedical Writer - RemoteNew York, NYRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Medical Writer - Perlmutter Cancer Center Clinical Trials Office NYU Langone Medical CenterMedical Writer - Perlmutter Cancer Center Clinical Trials OfficeNew York, NY$84,577.92–$88,200 / yearThe Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.
Medical Writer IPG MediaBrandsMedical WriterNew York, NY$82,000–$98,000 / yearEvaluate the following and take prompt and appropriate action where inadequacies are identified: datapackage, updates to medical literature, own work and effective and efficient management of projectresources (project box, scheduling, background information, databases, document tracking, and division of work within project team). Produce a range of written communications items in accordance with the needs of the client, target audience, target publication medium and level of design/creativity.
Medical Writer IPG Health Medical CommMedical WriterNew York, New YorkEvaluate the following and take prompt and appropriate action where inadequacies are identified: datapackage, updates to medical literature, own work and effective and efficient management of projectresources (project box, scheduling, background information, databases, document tracking, and division of work within project team). Produce a range of written communications items in accordance with the needs of the client, target audience, target publication medium and level of design/creativity.
Medical Writer - Perlmutter Cancer Center Clinical Trials Office NYU Langone HealthMedical Writer - Perlmutter Cancer Center Clinical Trials OfficeNew York, NY$84,577.92–$88,200Full timeThe Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.
Principal Medical Writer Revolution Medicines IncPrincipal Medical WriterNY$201,000–$251,000 / 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. Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.
Medical Writer WebMD Health CorpMedical WriterNY$82,500–$90,000 / yearMedscape, a division of WebMD, develops and hosts physician portals and related mobile applications that make it easier for physicians and healthcare professionals to access clinical reference sources, stay abreast of the latest clinical information, learn about new treatment options, earn continuing medical education credits and communicate with peers. An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; minimum of a Bachelor of Science degree (life sciences, public health, or clinical sciences) or similar with several years' relevant work experience required.
Senior Medical Writer (Remote) MMSSenior Medical Writer (Remote)Jersey City, NJRemoteWrite and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Senior Medical Writer (Remote - US) MMSSenior Medical Writer (Remote - US)New York, NYRemote$110,000–$120,000 / yearWrite and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Senior Medical Writer Katalyst HealthCares & Life Sciences IncSenior Medical WriterSouth Plainfield, NJResearches, authors, and/or edits complex clinical, scientific, and program-level regulatory documents, which may include Investigator's Brochures (IBs), Investigational New Drug (IND) application documents, and Marketing Authorization Application (MAA) documents. Serves as a primary author, providing strategic input and authoring regulatory documents supporting Phase 1-3 clinical drug development, including clinical study protocols, protocol amendments, and Clinical Study Reports (CSRs).
Medical Writer Flywheel PartnersMedical WriterNew York, NY$80,000–$85,000 / yearDESCRIPTION Flywheel (flywheelpartners.com) is a communications, education and training agency that supports leading healthcare companies by developing innovative medical and science educational resources – including but not limited to, eLearning modules, slide presentations, product brochures, backgrounders, videos, podcasts, learning games and skills development workshops. Consult with client project owners and subject matter experts (SMEs) to create engaging and effective educational content covering a broad range of topics—pharmaceutical drugs, medical and scientific information (ie, anatomy & physiology, disease state, diagnosis, treatment, marketplace), market access, the business of healthcare, and selling skills/soft skills.
Medical Writer Mediabrands Worldwide IncMedical WriterNew York, NY$82,000–$98,000 / yearEvaluate the following and take prompt and appropriate action where inadequacies are identified: datapackage, updates to medical literature, own work and effective and efficient management of projectresources (project box, scheduling, background information, databases, document tracking, and division of work within project team). Produce a range of written communications items in accordance with the needs of the client, target audience, target publication medium and level of design/creativity.
Principal Medical Writer BeOne Medicines AGPrincipal Medical WriterNY$119,300–$159,300 / yearGeneral Description: This position is responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. Essential Functions of the Job: Document Writing: Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.
Medical Writer I, II Or III Mitsubishi Tanabe PharmaMedical Writer I, II Or IIIJersey City, NJTypical duties would include substantive editing and review, researching and obtaining published reports on studies in a variety of different indications, writing executive summaries, and coordinating the publication of key preclinical and clinical scientific data through peer-reviewed journals and forums. Prepares clinical reports, summary documents, investigator's brochures, package inserts, protocols and protocol amendments, and other documents that may be submitted to the Food and Drug Administration (FDA) and the European Medicines Agency (EMEA) for publication and/or presentation.