133 Results for

Medical Writer Jobs in Uptown, NJ

Jobs

New!

New Brunswick, NJ1 day ago

$42.85–$45.45 Per Hour

strong>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.

New!

Florham Park, NJ1 day ago

Remote

$83.52–$83.52 Per Hour

div style="text-align:center"> www.onboardusa.com

. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.

NY30+ days ago

Remote

$85,000–$95,000 Per Year

Write 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.

New!

Florham Park, NJ1 day ago

Remote

$75–$81.71 Per Hour

li>Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products.

Manage the assigned writing tasks and ensure that the documents adhere to relevant regulatory guidelines, as well as SOP/WI(s), template(s), and style guide.

New!

Florham Park, NJ1 day ago

Remote

$71–$81 Per Hour

Manage the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as company's SOP/WI(s), template(s), and style guide.

Cedar Knolls, NJ30+ days ago

Remote

$160,000–$170,000 Per Year

With over 20 years of expertise in diagnosing rare disorders and diseases, and pioneering work in the identification of new disease-causing genes, our commitment to genetic disease detection, discovery, and diagnosis is based on sound science and is focused on enhancing patient care. Through both internal research efforts and global collaborations, we have identified and published hundreds of new disease-gene relationships and developed novel tools for genomic data analysis.

New!

Florham Park, NJ1 day ago

Primary Responsibilities: " Manage the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as SOP/WI(s), template(s), and style guide. " Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products.

NY30+ days ago

$100,600–$151,000 Per Year

Essential functions of the job include but are not limited to: Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidances . 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.

8 days ago

Remote

$95,000–$105,000 Per Year

You 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.

New!

Florham Park, NJ1 day ago

Remote

$75–$81.70 Per Hour

We'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.

New!

Jersey City, NJ1 day ago

Remote

Full-time

Write 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.

NY30+ days ago

Remote

$80,000–$110,000 Per Year

li>You conduct outstanding literature searches - using appropriate search strategy, keywords, and a variety of sources when researching journal articles, and medical research papers. 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.

New!

Jersey City, NJ1 day ago

$125,000–$136,800 Per Year

ul>

Independently write clinical and regulatory documents, including (but not limited to): clinical protocols, clinical study reports (CSRs), investigator brochures (IBs), common technical document (CTD) modules (Module 2.7.Xs, 2.5, and Module 5 integrated summaries), briefing documents, posters, abstracts, manuscripts and other documents per company and regulatory guidelines.

Take ownership of a given assignment, proactively consulting other cross-functional project team members to align and build consensus on timelines, document interdependencies, organize and drive kick off meetings, comment resolution meetings, and ad-hoc meetings to mitigate risks and resolve project related issues.

Jersey City, NJ30+ days ago

$148,000–$161,500 Per Year

Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases.

NY27 days ago

$119,300–$159,300 Per Year

General 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.

Westfield, NJ30+ days ago

$130,000–$140,000 Per Year

p>• Perform 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.

NY30+ days ago

$180,000–$202,000 Per Year

Author, review, and coordinate key clinical and regulatory documents for the 4D‑150 Phase 3 program as well as for the early-phase lung program, including but not limited to protocols, protocol amendments, CSRs, IBs, DMC materials, briefing documents, and BLA‑enabling content. This role is responsible for the planning, development, and delivery of high‑quality clinical and regulatory documents across late‑stage development, working closely with Clinical Science, Clinical Operations, Data Science, Regulatory Affairs, Quality, and external partners.

Jersey City, NJ30+ days ago

$82,000–$98,000 Per Year

Where an employee or prospective employee is paid within this range will depend on, among other factors, actual ranges for current/former employees in the subject position; market considerations; budgetary considerations; tenure and standing with the company (applicable to current employees); as well as the employees/applicants background, pertinent experience, and qualifications. We transform complex science into compelling healthcare communications and fuel the conversations within the medical community that help make a tangible difference to patients.

NY21 days ago

$93,000–$122,000 Per Year

Where an employee or prospective employee is paid within this range will depend on, among other factors, actual ranges for current/former employees in the subject position; market considerations; budgetary considerations; tenure and standing with the company (applicable to current employees); as well as the employee's/applicant's background, pertinent experience, and qualifications. We transform complex science into compelling healthcare communications and fuel the conversations within the medical community that help make a tangible difference to patients.

Wayne, NJ30+ days ago

The 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.

NY22 days ago

$137,100–$182,100 Per Year

New York, New York30+ days ago

Remote

Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.

Closing:

At MSK, we believe in fair, competitive pay that reflects your job, experience, and skills.

NY13 days ago

Remote

$94,640–$118,300 Per Year

Drawing on your technical writing background and managerial expertise, you analyze forecasts, track variances, and assign tasks to optimize project outcomes and resource allocation, and you offer insights and strategic approaches to enhance team effectiveness. Proven experience leading documentation efforts for information technology teams, technical staff, or similar groups, or demonstrated success managing teams and guiding complex projects in a related field.

NY30+ days ago

$18.50–$42.35 Per Hour

Our teams reflect the customers, patients, members and communities we serve and we are committed to fostering a workplace where every colleague feels valued and that they belong. At CVS Health, you'll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do.

NY30+ days ago

$90,000–$130,000 Per Year

p>Preferred:

Experience with large healthcare datasets (EHR, claims, monitoring data) Knowledge of IRB processes and regulatory requirements Experience with digital health, virtual care, or outcomes research Prior authorship in CV journals or presentations at major cardiology conferences (ACC, AHA, HRS, ESC).

Required:

Advanced degree (MD, PhD, MPH, MS, or equivalent) Experience conducting clinical research or real-world evidence studies Strong statistical and data analysis skills Demonstrated experience writing and publishing peer-reviewed manuscripts Familiarity with cardiovascular clinical research preferred.

Giralda Farms, NJ30+ days ago

$64–$68.45 Per Hour

Reporting 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.

New York, NY7 days ago

$90,000–$105,000 Per Year

Since 2004, PMC has been a pioneer in digital media reaching viewers on all screens across its ever-growing constellation of iconic brands, which includes Variety, Rolling Stone, The Hollywood Reporter, Billboard, Dick Clark Productions, WWD, SHE Media, Robb Report, Deadline, TVLine, Sportico, BGR, ARTnews, Fairchild Media, Vibe, IndieWire, Artforum, Gold Derby, and Luminate, the premier data and analytics company. For more information on the company, please visit www.

New York, NY17 days ago

For more information on the company, please visit www. Since 2004, PMC has been a pioneer in digital media reaching viewers on all screens across its ever-growing constellation of iconic brands, which includes Variety, Rolling Stone, The Hollywood Reporter, Billboard, Dick Clark Productions, WWD, SHE Media, Robb Report, Deadline, TVLine, Sportico, BGR, ARTnews, Fairchild Media, Vibe, IndieWire, Artforum, Gold Derby, and Luminate, the premier data and analytics company.

NY30+ days ago

$55–$75 Per Hour

Author, revise, and maintain user manuals for all Therabody devices including but not limited to percussive therapy, heating and cooling, pneumatic compression, light therapy, and electrical stimulation devices. Therabody is seeking a detail-oriented Contract Technical Writer to own the creation and maintenance of product documentation, safety documentation, and unit warning content across our full portfolio of consumer wellness devices.

New Brunswick, NJ30+ days ago

$40–$42 Per Hour

strong> Primary 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.

NY29 days ago

$155,300–$258,900 Per Year

Our research, by way of regular reports, topical commentaries and deep-dive empirical research, and our research presentations to clients and the investment and wealth ecosystem, enhances our engagement with clients, including asset owners, asset managers, ETF issuers and wealth channels. The team publishes insights on current market dynamics across global regions and asset classes (e.g., equities, equity factors, fixed income, multi-asset, cross-asset, wealth, asset allocation, portfolio construction dynamics).

Madison, New Jersey30+ days ago

£113,102–£141,396

Ensure 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.

NY14 days ago

Remote

$70,000–$80,000 Per Year

The team oversees the global product marketing strategy for Motorola Solutions' entire portfolio, develops the messaging and go-to-market strategy for the business, creates and drives marketing programs and campaigns aimed to generate leads and builds brand awareness among target audiences, including system integrators, end-users and consultants.

Research, write, and edit content across multiple formats including blog posts, articles, guides, white papers, web pages, email campaigns, datasheets, video scripts, ad copy, social media posts, and event and conference presentations.

NY30+ days ago

$42.61–$53.36 Per Hour

As champions of audio, we connect with people in the moments that matter - delivering trusted local news, passionate sports and your favorite music across 220+ radio stations, premium podcasts, live events and digital experiences that reach more than 200 million listeners every month. You must have the ability to assign and write for major breaking news stories, tragedies, lighter stories, celebrities, newsmakers, and thrive in an environment where your work is subject to intense public scrutiny.

Berkeley Heights, NJ23 days ago

$71,250–$114,000 Per Year

In 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.

New York, NY30+ days ago

$1,700–$2,000 Per Year

This often means working across Engineering Security and Technology Product Owners, collaborating closely with Legal Compliance and Risk, engaging Product and Data teams on technology risk considerations, and translating complex regulatory expectations into approaches that engineers can actually use. Youll work closely with the Global Head of Policy, engineering leadership, Risk, and Compliance partners, and subject matter experts across the organization to draft, socialize, and publish documentation.

USA, NY13 days ago

$70,000–$80,000 Per Year

This individual will play a critical role in securing and sustaining the financial resources that allow our mission to scale - crafting compelling narratives that connect funder priorities to the real-world impact of our work. Support the Enterprise and Impact teams in maintaining positive relationships with current and prospective funders through professional communication and stewardship.

New Hyde Park, NY30+ days ago

Full-time

We remain competitive by offering a wide range of logistics services, including: ocean and air freight, rail, trucking, warehousing and distribution, customs brokerage, cargo insurance and more. Ensures that all entries are properly classified by using tools such as company profiles, CROSS (Customs Rulings Online Search System), Internet and communicating with the Importer of record.

New York, New York30+ days ago

It’s not often that you can get in on the ground floor of a funded (unicorn!) startup that’s scaling.

Will leverage customer interactions and product usage data, and will identify opportunities for new or enhanced documentation and act as an advocate for customers by ensuring that documentation provides practical, actionable solutions to real-world challenges.

New!

NY6 days ago

$123,250–$166,750 Per Year

p>Role Description:

As a release readiness engineer and technical writer, you will develop and evolve the operator- and administrator- customer-facing documentation for UDS capabilities, enabling Warfighters and system administrators in installation, administration, operational runbooks, SDKS, and training content designed for airgapped environments.

Installation & deployment documentation: Create step-by-step install/configuration guides for product components and integrations (including prerequisites, expected outputs, verification steps, and safe rollback guidance).

New York, NY8 days ago

$80,000–$90,000 Per Year

To learn more about what it's like to work at EMARKETER check out our careers page and life page.

If this sounds like a great job for you, please apply online and tell us a bit about why you're a good fit for the role..

US pay range

$80,000—$90,000 USD

About EMARKETER

EMARKETER is the world's leading research company focused on digital transformation.

New York, NY30+ days ago

$120,000–$180,000

p>After successfully opening our flagship Institute in New York in 2022 and expanding to South Florida in 2024, we are now bringing the Atria experience to the West Coast with the launch of our Los Angeles Institute in late spring 2026.

You have 5-7 years of experience writing UX copy for consumer-facing digital products, and a portfolio that demonstrates it — including end-to-end case studies showing how you took a feature from concept to shipped copy.

NY30+ days ago

$90,000–$100,000 Per Year

The Senior Writer is responsible for developing relevant, memorable and highly creativecommunications for clients through language and ideas that support strategy, design, and brand expression. Interact closely with Designers and Creative Directors to create and refine content for a chosen design direction, identifying alternative message strategies for achieving clients' objectives.

New York City, NY17 days ago

$85,000–$160,000 Per Year

Working with senior members of the Strategy Team, you will develop a deep understanding of potential partners' transportation challenges and goals, learn Via's unique technical and operational strengths, and coordinate high-quality written proposals for effective shared mobility services.

Our teams of world-class engineers, data-scientists, product managers, operations specialists, marketers, transit experts and more bring cutting-edge AI-powered software and innovative technology-enabled operations to our partners across the globe.

NY30+ days ago

Remote

$53,000–$82,813 Per Year

Through our trusted brands, including the USA TODAY NETWORK, comprised of the national publication, USA TODAY, and local media organizations, including our network of local properties, in the United States, and Newsquest, a wholly-owned subsidiary operating in the United Kingdom, we provide essential journalism, local content, and digital experiences to audiences and businesses. They will craft compelling storytelling around games and puzzles, write and edit promotional and explanatory content, lead a weekly Play newsletter, write stories around horoscopes and comic releases, and work closely with product, growth and design teams to help shape the future of USA TODAY's games ecosystem.

New York, NY30+ days ago

$82,500–$97,000 Per Year

As Associate Manager, Institutional & Government Grant Writer, you will translate Uncommon Schools work into clear, compelling proposals that secure critical funding for our mission. Uncommon Schools is a nonprofit network of high-performing public charter schools dedicated to providing an exceptional K-12 education in economically disadvantaged communities.

NY30+ days ago

$60,000–$93,750 Per Year

Through our trusted brands, including the USA TODAY NETWORK comprised of the national publication USA TODAY and local media organizations, including our network of local properties in the United States and Newsquest, a wholly-owned subsidiary operating in the United Kingdom, we provide essential journalism, local content, and digital experiences to audiences and businesses. Reporting to the New Media Editor, this role centers on covering the evolving YouTube landscape, including top creators, trending shows, and breaking news in the YouTube space.

NY30+ days ago

$60,000–$93,750 Per Year

USA TODAY Entertainment is seeking a creative and trend-savvy New Media Writer/Reporter to cover the fast-evolving world of influencers, podcasts, and digital creators.

NY19 days ago

$60,000–$80,000 Per Year

In this role, your daily tasks will include researching, pitching and writing multiple articles (round-ups, gift guides, product reviews, etc) for publication across FOX properties, including Fox News and FOX Weather. Under the FOX banner, we produce and distribute content through some of the world's leading and most valued brands, including: FOX News Media, FOX Sports, FOX Entertainment, FOX Television Stations and Tubi Media Group.

New York, NY30+ days ago

$135,200–$182,900 Per Year

From animators to writers, product designers to researchers, Design brings purpose, feeling, and delight to every interaction with our brand, inside the app and out. It's a big mission, and even though we've made a lot of headway, we still have work to do - and that's where you come in!

Duolingo's designers care about creating high-quality experiences that look and feel fun.

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Medical Writer Jobs in Uptown, NJ

Quality - Technical writer ECLARO

Senior Medical Writer On-Board Companies

Medical Writer, Accredited Medical Education MJH Healthcare Holdings LLC

Senior Medical Writer Artech LLC

Senior Medical Writer Primary Talent Partners

Principal Medical Writer GeneDX LLC

Senior Medical Writer III Integrated Resources, Inc

Senior Medical Writer Precision Medicine Group LLC

Principal Medical Writer MJH Healthcare Holdings LLC

Senior Medical Writer Net2Source

Senior Medical Writer (Remote) MMS

Medical Writer, Medical Communications Precision Medicine Group LLC

Senior Medical Writer I Eikon Therapeutics Inc

Senior Medical Writer II Eikon Therapeutics Inc

Principal Medical Writer BeOne Medicines AG

Medical Writer Tata Consultancy Services Ltd

Principal Medical Writer 4D Molecular Therapeutics Inc

Medical Writer IPG Health LLC

Senior Medical Writer IPG Health LLC

Medical Records Summary Writer- In person position Advanced Orthopaedic Associates Of

Senior Principal Medical Writer BeOne Medicines AG

Editor/Grant Writer, Department of Surgery Memorial Sloan Kettering Cancer Center

Technical Writer, Manager Acentra Health

Senior Document Writer CVS Health Corp

Clinical Research Writer Heartbeat Health Inc

Nonclinical Regulatory Document and Scientific Writer Artech LLC

SHE Media: Senior Writer, Health & Wellness Penske Media Corp.

PMC: E-Commerce Writer Penske Media Corp.

Technical Writer, Contract Therabody Inc

Technical writer Sunrise Systems Inc

Investment Research Writer, Global Investment Research London Stock Exchange Group Plc

Scientific Writer - Translational Development RD Partners

Digital Content Writer - Digital Marketing Motorola Solutions Inc

Editor/Writer WINS (part time) Audacy Inc

Senior Technical Writer Fiserv Inc

Technology Policy Writer - Engineering COO Office Contract Bloomberg LP

Grant Writer PCs for People

Senior Customs Entry Writer OEC Group

Technical Writer | Housing EliseAI

Release Readiness Engineer / Technical Writer Defense Unicorns, Inc

Media Content Analyst/Writer EMARKETER

UX Writer Atria Health and Research Institute

Senior Writer VSA Partners LLC

Senior Proposals Writer Via

Play Writer USA TODAY Co Inc

Associate Manager, Institutional & Government Grant Writer UNCOMMON SCHOOLS, INC.

YouTube Writer/Reporter, USA Today Entertainment USA TODAY Co Inc

New Media Writer/Reporter, USA TODAY Entertainment USA TODAY Co Inc

Writer, Commerce Fox Corp

Product Writer Duolingo Inc

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