NewCustoms Entry Writer JobotCustoms Entry WriterMoonachie, NJ$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.
Quality - 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.
NewAssociate Director, Medical Writing - Publications JouléAssociate Director, Medical Writing - PublicationsRaritan, NJRemote$160,000–$165,000 / yearProvide expert writing and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at meetings. A PhD, MD, or PharmD with a minimum of 5 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 8 years relevant pharmaceutical/scientific experience is required.
NewSr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos HealthSr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredNew JerseyProvides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission documents) accurately and consistently present key data-driven clinical messages in accordance with program goals and regulatory requirements. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success.
Medical Writer Systimmune IncMedical WriterPrinceton, NJ$80,000–$130,000 / yearPosition Summary: The 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. Key Responsibilities: 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.
Senior Medical Writer Net2SourceSenior Medical WriterFlorham Park, NJRemote$75–$81.70 / hourWe're looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress. At Organon, you'll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a Fortune 500 company with an international footprint that serves people in more than 140 markets.
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 Knowesis, Inc.Medical WriterEast Orange, NJ$85,000–$89,000 / yearDevelop, write, and edit a wide range of clinical, scientific, and research-based documents, including study protocols, leadership reports, manuscripts for publication, regulatory submissions, grant proposals, and other technical materials essential to research and clinical operations. Maintain up-to-date VHA-required training for all personnel involved in patient care and/or research studies, including but not limited to: VA Privacy and Information Security Awareness and Rules of Behavior; VHA Privacy Policy Web Training; and Collaborative Institutional Training Initiative (CITI) Program Training.
Senior Medical Writer (Remote) MMSSenior Medical Writer (Remote)Jersey City, NJRemoteFull timeWrite 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.
Associate Medical Writer MJH Healthcare Holdings LLCAssociate Medical WriterCranbury, NJ$65,000–$75,000 / yearThe 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 WriterCranbury, New JerseyComprehend and apply relevant evidenced-based medical literature, clinical practice guidelines, and disease-state information for the development of content across various therapeutic areas (eg, identify levels of evidence, clinical trial data, clinical utility of therapeutic choices and unmet needs in treatment landscapes, product-specific education). As a Medical Writer with the Enterprise Content Team at MJH Life Sciences®, you will play a vital role in developing educational content for healthcare professional audiences.
Medical Writer SystimmuneMedical WriterPrinceton, NJFull timeThe 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 III Johnson & JohnsonMedical Writer IIITitusville, NJ$109,000–$174,800 / yearAll Job Posting Locations: Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Medical Writer Oxford Global Resources, LLCMedical WriterRaritan, NJCompensation $55.00 - $55.00 / Hourly ### Hours Per Week 40 ### Number Of Positions 1 ### Job Description Summary: The purpose of this role is to write, or coordinate the preparation of, all clinical, regulatory and scientific documents intended to support clinical and regulatory deliverables for drug development project teams. The scope of the role includes authoring, review, and quality assurance check of documents, and management of external medical writers.
Medical Writer Tata Consultancy Services LtdMedical WriterWestfield, NJ$130,000–$140,000 / yearPerform exhaustive Medical and Regulatory review of content respect to ensure Medical and Regulatory accuracy, consistency with references, sequencing and accuracy of bibliography references and ensure the scientific information in branded or promotional content is current, valid and adheres to the respective countrys pharma regulations. • To Check the Scientific accuracy and correctness of content to ensure whether content is adequately supported by evidence, depicted tables/graphs and artwork accurately represent the data and there are no contradictory messages in the body of the content.
Hybrid Medical Writer Inizio EngageHybrid Medical WriterTitusville, New JerseyAs needed, provide medical review for scientific accuracy and provide input on the development/use of scientific and promotional materials consistent with approved client processes and policies (Product Review Committee [PRC], Reprint Dissemination Committee[RDC]) and in close partnership with client Medical Content Strategy Leads and MI leadership team to identify and address training needs of Medical Information and Communications staff, internal partners, or external vendors. Our passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people, and providers to improve treatment outcomes.
Medical Records Summary Writer- In person position Advanced Orthopaedic Associates OfMedical Records Summary Writer- In person positionWayne, NJThe Medical Records Summary Writer (internally called a Quality Assurance Coordinator) is responsible for reviewing and extracting pertinent medical information from prior medical records and creating a well written summary. • Must demonstrate exceptional communication skills by conveying necessary information accurately, listening effectively and asking questions where clarification is needed.
NewExpert 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.
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.
Senior Technical Writer Aditi ConsultingSenior Technical WriterHoboken, NJRemote$56–$57 / hourConsent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. The User Assistance team for Higher Ed creates user-focused, data-informed, accessible, web- and mobile-based content to help students and educators use our products to accomplish their goals.
Grant Writer – Workforce & Career Training Programs American Medical and Trade InstituteGrant Writer – Workforce & Career Training ProgramsPassaic, NJRemoteThe role requires close coordination with AMTI leadership to ensure grant proposals align with existing certification programs such as Certified Medical Assistant (CMA), Phlebotomy Technician, EKG, and criminal justice pathways, as well as managing submission timelines and post-award requirements when applicable. This includes researching federal, state, county, workforce, and education-adjacent funding sources; preparing competitive grant narratives and budgets; and positioning AMTI appropriately as a program provider, fiscal agent, or contracted partner.
Technical writer Sunrise Systems IncTechnical writerNew Brunswick, NJ$40–$42 / hourPrimary Responsibilities: Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
NewTechnical Writer 2 OracleTechnical Writer 2Trenton, NJ$31.83–$63.65 / hourOracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Work in accordance with corporate and organizational security policies and procedures, understand personal role in safeguarding corporate and customer assets, and take appropriate action to prevent and report any compromises of security within scope of position.
Senior Technical Writer Fiserv IncSenior Technical WriterBerkeley Heights, NJ$71,250–$114,000 / yearIn this role, you will also provide guidance to junior writers, support training and knowledge sharing, and lead documentation efforts across assigned workstreams to improve content quality, usability, and consistency across modern delivery platforms. You will work with product, support, and artificial intelligence teams, along with subject matter experts, to create modular documentation that supports intelligent search, automation, and chatbot experiences.
Associate Report Writer GeneDX LLCAssociate Report WriterCranbury, NJRemote$90,000–$118,000 / yearWith a focus on accuracy, scientific rigor, and cross-functional communication, the Associate Report Writer supports team objectives, maintains current knowledge of best practices, and helps facilitate timely and reliable reporting. The role contributes to the curation of internal variant databases, collaborates with clinical and laboratory teams, and may serve as a subject matter expert for specific genes, disorders, or workflows.
Grant Writer & Grant Compliance Administrator NjtransitGrant Writer & Grant Compliance AdministratorNewark, NJSUMMARY: Candidate will be responsible for drafting high-quality, comprehensive competitive grant applications for submission to federal and state funding agencies and ensuring that statutory and administrative requirements are met prior to application submission. EDUCATION, EXPERIENCE AND QUALIFICATIONS: Bachelor's degree in Business or Public administration and three (3) years of grant administration/management, technical/business writing experience or any combination of the beforementioned.
Technical Writer - Operations Experic LLCTechnical Writer - OperationsCranbury, NJ$80,000–$110,000 / yearThis role will partner closely with Manufacturing, Packaging, Warehouse, Facilities, and Quality Assurance teams to draft, revise, route, and maintain controlled documentation in support of compliant GMP operations. Drafts, revises, formats, and coordinates controlled GMP documentation including: Coordinates document review, approval, and implementation activities between Operations and QA.
NewAutomotive Service Advisor-Writer / Quick Lube Jiffy LubeAutomotive Service Advisor-Writer / Quick LubeTrenton, NJThe service advisor must be able to analyze, comprehend and recommend financial objectives that increase sale and service results energized by face-to-face interaction with guests, to include resolving any issues, and help increase sales and build loyalty. Service Advisors must expect to stand for long periods of time on hard surfaces, like concrete or metal, and expect to work in an environment in which you may frequently experience hot and cold temperatures, loud noises, and exhaust fumes.
Technical Writer Actalent IncTechnical WriterSomerset, NJ$30–$40 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. This role focuses on creating clear, accurate, and user-friendly technical documentation that supports complex capital and semiconductor equipment used worldwide.
Service Writer Brakepoint LLCService WriterTabernacle, NJThe Service Writer will be responsible for coordinating and facilitating all communication between customers and our service department to ensure a seamless and efficient service experience. - Greet customers and assist them with scheduling service appointments, explaining services, and answering any questions they may have.
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.
R-168896 Full Time Nabisco Merchandiser/Order Writer - Kearny, NJ Mondelez InternationalR-168896 Full Time Nabisco Merchandiser/Order Writer - Kearny, NJKearny, New Jersey$22.62–$24.62As a Brand Execution Merchant, you’ll bring world-famous snacks like Oreo, Ritz, belVita, Chips Ahoy!, and Triscuit to life in-store – building relationships, stocking shelves, executing displays, and ensuring shoppers always find their favorite snacks right where they expect them. We're leading the future of snacking with iconic global and local brands such as Oreo, Ritz, LU, Clif Bar and Tate's Bake Shop biscuits and baked snacks, as well as Cadbury Dairy Milk, Milka and Toblerone chocolate.
Training Specialist & Technical Writer - (Data Center Cooling Solutions) nVent Electric PlcTraining Specialist & Technical Writer - (Data Center Cooling Solutions)NJRemote$76,000–$141,100 / yearWe provide a broad benefits package with meaningful programs for eligible full-time employees that includes: Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation.
Senior Technical Writer CQ Medical CareersSenior Technical WriterVirtual, New JerseyDevelop and Write Labeling Content: Create, write, and edit high-quality, clear, concise, and accurate labeling materials for medical devices, including product labels, user manuals, instruction guides, and packaging inserts. Collaborate with Design and Engineering Teams: Work with product development, engineering, and design teams to understand product specifications, functionality, and key messages that should be included in the labeling.
Technical Writer Marotta Controls, Inc.Technical WriterParsippany, NJ$75,000–$100,000 / yearThe team designs and develops valves and fluid control products for launch vehicles, spacecraft, satellites, and space station applications. The Technical Writer will create and maintain technical documentation to support new product development, training initiatives, and legacy programs.
NewAutomotive Service Advisor - Writer OPEN ROAD AUTO GROUPAutomotive Service Advisor - WriterEast Brunswick, NJFull timeAs an Automotive Service Advisor, you'll play a critical role in creating positive customer experiences while helping drive service department success. In this role, you'll help ensure every customer receives outstanding service while contributing to the success of a busy, high-performing dealership.
NewFull Time Nabisco Merchandiser/Order Writer Mondelez International IncFull Time Nabisco Merchandiser/Order WriterMarlboro, NJ$22.55–$24.55 / hourWe have corporate offices, sales, manufacturing and distribution locations throughout the U.S. to ensure our iconic brands-including Oreo and Chips Ahoy! cookies, Ritz, Wheat Thins and Triscuit crackers, and Swedish Fish and Sour Patch Kids confectionery products -are close at hand for our consumers across the country. Represent Mondelz in front of in-store employees and work closely with sales representatives to optimize the visibility of Mondelz products on shelves and to construct promotional displays.
NewAutomotive Service Advisor Writer Jiffy LubeAutomotive Service Advisor WriterTrenton, NJMust be able to operate equipment such as overhead and floor mounted oil and grease guns, transmission machine, air conditioner service machine, radiator service machine, hand tools and basic shop equipment. Must be able to push, pull, lift, and bend at the knees and waist, twist body at the waist, raise and hold arms overhead, and turn head-neck-shoulders as needed.
Automotive Service Advisor/Writer George Wall FordAutomotive Service Advisor/WriterRed Bank, New JerseyWe are proud to be the highest volume Ford dealer in Monmouth and Ocean counties and one of the highest volume in all of NJ, while continuing to earn Ford's most prestigious honor for it's dealers, the President's Award. Prior Ford and Reynolds & Reynolds experience is preferred for this position as it is pivotal that our technicians and advisors can effectively communicate not only with each other, but with our customers as well.
Automotive Service Advisor - Writer Jiffy LubeAutomotive Service Advisor - WriterBridgewater Township, NJ$19–$20Must be able to operate equipment such as overhead and floor mounted oil and grease guns, transmission machine, air conditioner service machine, radiator service machine, hand tools and basic shop equipment. In the early days, Jiffy Lube provided oil & fluid maintenance and [now] almost every common major and minor repair service - from brakes to tires to suspensions to engine-diagnostics and more.
NewSenior AI Prompt Writer SitusAMCSenior AI Prompt WriterTrenton, NJRemote$100,000–$130,000 / yearThis position is instrumental in translating complex business needs into actionable AI use cases, developing and reviewing test plans, and leading quality assurance, volume, and bias testing to ensure the reliability and ethical integrity of AI models and processes. Assist in defining and refining acceptance criteria and success measures for backlog tickets to ensure clarity, testability, and alignment to expected outcomes.
Automotive Service Advisor-Writer Jiffy LubeAutomotive Service Advisor-WriterFanwood, NJ$19Must be able to operate equipment such as overhead and floor mounted oil and grease guns, transmission machine, air conditioner service machine, radiator service machine, hand tools and basic shop equipment. In the early days, Jiffy Lube provided oil & fluid maintenance and [now] almost every common major and minor repair service - from brakes to tires to suspensions to engine-diagnostics and more.
NewSenior Technical Writer MedTec LLCSenior Technical WriterNJDevelop and Write Labeling Content: Create, write, and edit high-quality, clear, concise, and accurate labeling materials for medical devices, including product labels, user manuals, instruction guides, and packaging inserts. Collaborate with Design and Engineering Teams: Work with product development, engineering, and design teams to understand product specifications, functionality, and key messages that should be included in the labeling.
NewSr. Medical Editor (Regulatory Documents + QC) - US Home based Syneos HealthSr. Medical Editor (Regulatory Documents + QC) - US Home basedNew JerseyServes as project lead for deliverables of assigned complex and/or large medical writing projects, including, but not limited to, scheduling and leading internal project-specific team meetings, organizing project-specific requirements, and ensuring all information is distributed to the editorial team and implemented within the deliverable. •Copyedits assigned documents, applying correct grammar, punctuation, spelling, and style following AMA Manual of Style or various custom style guidelines as well as established medical writing internal checklists and best practices.
Sr. Manager, Medical Writing Terumo Medical CorpSr. Manager, Medical WritingSomerset, NJ$150,000–$198,000 / yearD, MA/MS or MPH) in a medical/biomedical/scientific discipline with a minimum of 5 years of experience in medical writing of regulatory documentation (clinical research documentation is optional) OR Bachelor's Degree, preferably in life sciences with 10 years of relevant work experience; OR equivalent combination of education, training and relevant experience. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients.
Director, Medical Writing Genmab ASDirector, Medical WritingPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Significant experience in working with drug development processes, Good Clinical Practice (GCP), regulatory requirements and guidelines associated with all regulatory documents (including CTA/IND submissions, protocols, investigator brochures, and clinical study reports).
Associate Director, Medical Writing Taiho OncologyAssociate Director, Medical WritingPrinceton, NJRemote$194,650–$229,000 / yearFull timeFDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Associate Director, Medical Writing GenmabAssociate Director, Medical WritingPrinceton, NJFull timeFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. This includes authoring briefing documents, clinical trial medical synopses, protocols, investigator's brochures, PIPs, CSRs, Health Authority briefing books, Health Authority responses, and other clinical documentation to support the conduct of trials and regulatory submissions/filings.
Director - North America Medical Affairs Hikma Pharmaceuticals PlcDirector - North America Medical AffairsBerkeley Heights, NJ$121,000–$220,000 / yearThe role serves as the strategic bridge between Hikma's R&D, Regulatory Affairs, Pharmacovigilance (PV), Quality, Commercial, Legal, and Compliance on the one hand and the external community of healthcare professionals, pharmacies, payers and insurers, medical boards and professional societies, health-system and policy decision makers, and patient advocacy groups on the other. The role oversees a focused but rapidly expanding footprint, including current in-house medical science liaison (MSL) coverage supporting an established hospital injectable product and upcoming launch programs requiring an MSL field team of approximately 1-5 professionals.