37 Results for

Medical Writer Jobs in Uptown, NJ

Jobs

Remote

$85,000–$95,000 / year

p>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.

30+ days ago

Remote

$80,000–$110,000 / 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.

30+ days ago

Florham Park, NJ

Remote

$83.52–$83.52 / 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.

4 days ago

$100,600–$151,000 / year

p>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.

30+ days ago

Florham Park, NJ

Remote

$75–$81.71 / 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.

4 days ago

Cedar Knolls, NJ

Remote

$160,000–$170,000 / 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.

30+ days ago

Remote

$95,000–$105,000 / 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.

11 days ago

Florham Park, NJ

Remote

$75–$81.70 / 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.

4 days ago

Jersey City, New Jersey

Remote

For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

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.

5 days ago

$119,300–$159,300 / 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.

30 days ago

Jersey City, NJ

$125,000–$136,800 / 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.

4 days ago

Jersey City, NJ

$148,000–$161,500 / 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.

30+ days ago

Westfield, NJ

$130,000–$140,000 / 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.

30+ days ago

Jersey City, NJ

$82,000–$98,000 / 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.

30+ days ago

$93,000–$122,000 / 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.

24 days ago

$180,000–$202,000 / 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.

30+ days ago

$137,100–$182,100 / year

p>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.

25 days ago

Wayne, NJ

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.

30+ days ago

Remote

$77,100–$119,400 / year

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. American Medical Writers Association (AMWA) Board of Editors in the Life Science University of Chicago Medical Writing & Editing Program certification preferred.

23 days ago

Remote

$94,640–$118,300 / 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.

16 days ago

New York, NY

Remote

$130,000–$160,000 / year

Oversee the planning, writing, editing, and quality control of a wide range of clinical and regulatory documents, including technical documentation for CE-IVDR/MDR, summaries, and responses to notified body questions, but also could include clinical study protocols, clinical study reports (CSRs), Investigator's Brochures (IBs), and similar documentation, as needed by the Clinical Development teams. Collaborate effectively with cross-functional teams including CCOE Clinical Development, Biostatistics, Data Management and Operating Company partners in Regulatory Affairs, Quality Assurance, Medical & Scientific Affairs and R&D to gather necessary input and ensure scientific accuracy and consistency across documents.

30+ days ago

$160,000–$180,000 / year

Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogees antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Collaborates with cross-functional teams to prepare, review, and edit high-quality, scientifically accurate, and submission-ready documents including, but not limited to: protocols, investigators brochures, clinical study reports, briefing documents, Module 2 summary documents, and other clinical and regulatory documents.

30+ days ago

$95,000–$130,000 / year

This role is a leader in the medical writing space who authors regulatory and clinical documents in accordance with internal procedures and global regulatory requirements, while leading collaboration with cross-functional stakeholders supporting clinical, regulatory, and business objectives. Skills: Advanced medical writing, clinical regulatory expert, project management, strong attention to detail, and expert with MS Office and reference management tools.

30+ days ago

Somerset, NJ

$150,000–$198,000 / year

D, 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.

29 days ago

$125,000–$140,000 / year

ul>

Excellent computer skills that include working remotely on shared networks and cloud-based systems (e.g., SharePoint, Google Drive, Workfront, and others) - Preference given to individuals proficient / experienced in using AI-driven tools and platforms.

An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; a Bachelor of Science degree (life sciences, public health, or clinical sciences) with several years' relevant work experience required.

30+ days ago

Pearl River, NY

$239,900–$399,800 / year

p>Support study team:

Provides clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team).
Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or;
An investigator with significant experience in vaccine clinical studies in academic, NGO or public health institutions may be considered.

30+ days ago

$130,000–$140,000 / year

p>As a Scientific Director with Clinical Communications, you will be working closely with an internal team dedicated to producing content for live event and sponsored video projects that will educate and inform oncology care provider audiences with the goal of improving outcomes of care.

Provide support as a subject matter expert for business development efforts; work collaboratively with sales associates to identify and present opportunities for supported projects and programs; participate in project management functions (eg, SOW, development of timelines, budgets, etc).

30+ days ago

New York, NY

$187,000–$205,000

li>10+ years of experience in clinical research or drug development, with sufficient protocol-level knowledge to understand and contextualize customer workflows; prior experience as a Clinical Scientist, Clinical Program Manager, Study Manager, CRA, CTM, or Data Manager at a sponsor, CRO, or clinical site is preferred.

Lead workshops with customer user groups (Clinical Scientists, Clinical Operations, Data Management, and Medical Writers) with a focus on end user training for self-sufficiency, empowering customers to independently leverage the Faro Platform.

18 days ago

New York City, NY

$139,100–$231,900 / year

Use innovative analytical methods to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states to optimize doses, dosage regimens and study designs throughout clinical drug development in collaboration with pharmacometrics and statistics (as relevant). Provide the clinical pharmacology components of Clinical Plans and provides clinical pharmacology expertise to the project team including plan, design and oversee clinical pharmacology studies with operational assistance from operations colleagues.

19 days ago

Tarrytown, NY

li> Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.

Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.

13 days ago

Newark, NJ

19 days ago

Remote

$161,000–$187,000 / year

Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Approximately 5+ years of relevant experience in scientific communications, medical communications, medical affairs, medical information, or a related biotech/pharma function.

30+ days ago

Rahway, NJ

$117,000–$184,200 / year

p>Required Skills:

Clinical Data, Clinical Protocol, Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trials, Clinical Trials Analysis, Data Analysis, Drug Development, ICH GCP Guidelines, Ophthalmology, Regulatory Compliance, Strategic Thinking. Under the direction of the Program Lead, you will collaborate with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.

5 days ago

$128,890–$156,179 / year

IPS conducts applied computational research in areas that include genomic, structural and molecular informatics, computational and systems biology, patient selection and translational biomarker research, and broader fields including knowledge science, epidemiology and machine learning-across the full lifecycle of drug discovery and development and across all therapeutic areas at BMS. This hands-on role partners closely with internal study teams, vendors, CROs, and cross-functional stakeholders to ensure research data are effectively managed as a strategic organizational asset, aligned with FAIR data principles, and positioned to meet AI-ready data goals.

3 days ago

Rahway, NJ

$173,200–$272,600 / year

p>Required Skills:

Data Analysis, Outcomes Research, Payer Evidence, Pharmaceutical Medical Affairs, Project Management, Real World Evidence (RWE), Scientific Communications, Scientific Publications, Scientific Reviews, Strategic Planning.

The Associate Director, Global Scientific & Value Content - Payor (AD, GSVC-Payor), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs and Outcomes Research.

30+ days ago

Remote

$173,700–$202,650 / year

The Senior Manager, Regulatory Writing is responsible for authoring regulatory documents, including but not limited to clinical study protocols, protocol amendments, clinical study reports (CSRs), clinical summaries, investigators brochures (IBs), pediatric documents, and regulatory authority briefing materials and responses. If a lead writer for assigned programs, serves as the primary point of contact for submission and project teams while acting as the lead author for complex documents while supporting document timelines and content strategy.

30+ days ago

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Medical Writer job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Medical Writer Jobs in Uptown, NJ

Medical Writer, Accredited Medical Education MJH Healthcare Holdings LLC

Medical Writer, Medical Communications Precision Medicine Group LLC

Senior Medical Writer On-Board Companies

Senior Medical Writer Precision Medicine Group LLC

Senior Medical Writer Artech LLC

Principal Medical Writer GeneDX LLC

Principal Medical Writer MJH Healthcare Holdings LLC

Senior Medical Writer Net2Source

Senior Medical Writer (Remote) MMS

Principal Medical Writer BeOne Medicines AG

Senior Medical Writer I Eikon Therapeutics Inc

Senior Medical Writer II Eikon Therapeutics Inc

Medical Writer Tata Consultancy Services Ltd

Medical Writer IPG Health LLC

Senior Medical Writer IPG Health LLC

Principal Medical Writer 4D Molecular Therapeutics Inc

Senior Principal Medical Writer BeOne Medicines AG

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

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

Technical Writer, Manager Acentra Health

Manager, Medical Writing Danaher Corp

Senior Manager, Medical Writing Apogee Therapeutics Inc

Medical Writing Manager Integra LifeSciences Holdings Corp

Sr. Manager, Medical Writing Terumo Medical Corp

Medical Science Director WebMD Health Corp

Clinical Development Medical Director Pfizer Inc

Scientific Director (Oncology) MJH Healthcare Holdings LLC

Director, Solutions Onboarding Faro Health Inc.

Associate Director, Clinical Pharmacology Pfizer Inc

Lead Statistical Programmer Katalyst Healthcares & Life Sciences

Lead Statistical Programmer Karwell Technologies

Senior Scientific Communications Manager Oruka Therapeutics Inc

Senior Scientist, Clinical Operations - Ophthalmology Merck & Co Inc

Research Data Coordinator Bristol-Myers Squibb Co

Associate Director, Global Scientific & Value Content - Payor (AD, GSVC-Payor) Merck & Co Inc

Senior Manager, Regulatory Writing Cytokinetics Inc

Resume Resources

Similar Job Searches