18 Results for

Author Jobs in Summit, NJ

Jobs

New Brunswick, NJ20 days ago

$42.85–$45.45 Per Hour
Full-time
Employee

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 York, NY18 days ago

$48.57–$50 Per Hour

The AEM Author is responsible for creating, editing, managing, and publishing digital content using Adobe Experience Manager (AEM). Skills: Category Name Required Importance Experience SkillCategoryTest1_MN Digital : Adobe Experience Manager (AEM) Yes 1 >7 years

Paramus, NJ13 days ago

$45–$49 Per Hour

This role bridges drug development, manufacturing, and quality control to deliver high-quality eCTD submissions. Compliance & Risk Management: Identify/escalate CMC regulatory risks and propose mitigation strategies.

Paramus, NJ30+ days ago

The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents. Collaboration & Review: Work closely with cross-functional teams, including medical, clinical, regulatory, statistical, and quality assurance teams.

New Brunswick, NJ26 days ago

o Primary Responsibilities: o 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. o 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 Brunswick, NJ26 days ago

$40–$42 Per Hour

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.

New Brunswick, NJ26 days ago

$33.03–$41.95 Per Hour

New!

Brooklyn, NYToday

$35–$45 Per Hour

Marketing content creation: Write and edit blog posts, long-form articles, whitepapers, reports, email campaigns, social media copy, and thought leadership content focused on the energy industry and EnergyHub's solutions. We collect and use those categories of Personal Information about you for human resources and other business management purposes, including identifying and evaluating you as a candidate for potential or future employment or future positions, recordkeeping in relation to recruiting and hiring, conducting analytics, and ensuring compliance with applicable legal requirements and Company policies.

New Brunswick, NJ26 days ago

$68,702–$87,256

This includes supporting Module 2.3 and Module 3 content, coordinating source documentation, managing submission timelines, reviewing and adjudicating comments, facilitating data verification, and helping ensure consistency and clarity across the dossier. This position requires close collaboration with Process Development, Analytical Development, Cell Therapy Technical Operations, Quality, Regulatory Sciences, CMC matrix team leaders, project management, document management, and external suppliers as needed.

NY30+ days ago

$90,000–$130,000 Per Year

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.

New York, NY12 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).

NY19 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.

Union, NJ30+ days ago

$45–$50

Experience authoring a variety of document types, including system design documents, project management-related plans, user guides/manuals, and training materials . Advanced skills using Microsoft Word (including creating, editing, deleting styles; track changes; and maintaining proper version control), Excel, and PowerPoint .

Springfield, NJ30+ days ago

This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry. Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.

New!

Long Island City, NY5 days ago

$62,000–$101,000 Per Year

Identify safety concerns, issues, incidents or hazards that should be reported and report them whenever possible and by any means necessary including JetBlue's confidential reporting systems (Aviation Safety Action Program (ASAP) or Safety Action Report (SAR)). When working or traveling on JetBlue flights, and if time permits, all capable crewmembers are asked to assist with light cleaning of the aircraft.

NY10 days ago

$122,600–$183,800 Per Year

This range represents our good faith expectation of what we reasonably expect to pay for this role based on factors including (but not limited to) skills, experience, training, licensure and certifications, education, and other business and organizational needs. Increasingly, organizations must reskill employees for ever-changing remote and hybrid work environments, create learning cultures that attract and retain employees in a tight labor market, and use training to build more equitable, empowering, and engaging workplaces.

NY30+ days ago

Remote

$95,000–$105,000 Per Year

In addition to representing the Clinical Communications team as a content expert, the Principal Medical Writer interfaces with clients, promotional review teams, key opinion leaders, and a variety of internal professional services. • Assist writers/editors on the team in workload prioritization with deliverables and timelines of projects, prioritizing timely delivery of high-quality content.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

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

Create A Free Account

Author Jobs in Summit, NJ

Quality - Technical writer Eclaro

AEM Author Varite, Inc

Pharmaceutical CMC Writer Macpower Digital Assets Edge Private Limited

Medical Writer Katalyst Healthcares & Life Sciences

Quality - Technical writer Mindlance

Technical writer Sunrise Systems Inc

Technical writer Integrated Resources, Inc

Contract Opportunity: Marketing Writer, Energy Sector EnergyHub

Regulatory CMC Technical Writer SOKOL GxP Services

Clinical Research Writer Heartbeat Health Inc

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

Technical Writer, Contract Therabody Inc

On Site Technical Writer - Union, NJ Adaptation

Technical Writer CEDENT

Writer Technical JetBlue Airways Corp

Sr. UX Writer II, Systems Articulate Global Inc

Principal Medical Writer MJH Healthcare Holdings LLC

Resume Resources