Trabajos content writer en New Jersey

Job Description Compensation: $500/month Best Version Media, a growing neighborhood magazine company, is looking for someone local to the Rumson area to coordinate content for a new magazine serving unique, upscale neighborhoods. According to hard monthly deadlines, the Content Coordinator is responsible for: • Finding a family or resident to be featured on the cover each month, • Interviewing residents, • Writing resident feature profiles, • Gathering, writing and editing local content, • Managing submissions from local contributors, • Formatting and uploading text and photos, • Proofreading magazines for grammar and spelling The ideal candidate must live in proximity to the area, have strong organization and communication skills, and enjoy writing. This is a work-from-home independent contractor position with flexible part-time hours. An ideal job for many people, including stay-at-home parents, teachers, university students and retirees. Training is provided.

Job Description Mandatory Skills - Technical Writer(US healthcare), Complete understanding of HL7 versions, and FHIR Key Responsibilities: The Senior Technical Writer & Specifications Analyst is a hybrid role responsible for performing technical business analysis—including requirements gathering and data mapping—and translating those requirements into high-quality, developer-facing API specification documentation. This individual owns the complete lifecycle of documentation for our integration and interoperability services, including orders and results services. Working directly with clinical, technical, product, and analysis teams, they will define data specifications, construct mapping sheets, and build clear, user-friendly documentation to help both internal consumer teams and external customers seamlessly integrate with Quest systems. The ideal candidate has deep expertise in healthcare standards (HL7 and FHIR) and a proven background in simplifying complex integration workflows. Key Responsibilities • Responsible for analysis, design, coding and testing of new applications or Partner with technical, development, and product teams to gather, define, and document technical requirements for new and existing interoperability services., • Create and maintain comprehensive, interactive API specification documentation (including schemas, endpoints, headers, and error codes) specifically for orders and results services., • Perform detailed data mapping, interface specification design, and clinical data flow analysis (e.g., mapping HL7 segments/fields and FHIR profiles)., • Develop and maintain technical guides, quick-starts, step-by-step tutorials, and release notes for both internal developers and external customer IT teams., • Validate technical specifications by actively testing APIs (using tools like Postman or cURL) and reproducing integration workflows to ensure accurate documentation., • Implement and manage a "Docs-as-Code" workflow, utilizing version control and markdown formatting to streamline review cycles and updates., • Collaborate during Agile backlog grooming and sprint planning to proactively identify documentation and interface specification needs early in the product lifecycle., • Standardize content across integration portals to ensure consistency, clarity, and adherence to both industry interoperability standards and brand style guides., • Promote an environment that encourages collaboration, initiative, continuous improvement, learning, and the generation of innovative ideas and solutions. Required Skills & Qualifications • 5 or more years of experience in technical writing, business systems analysis, or integration analysis, with progressive responsibilities in documenting APIs or clinical integrations., • 3 or more years of experience in healthcare interoperability, with a focus on electronic health records (EHRs) and clinical data exchange., • Demonstrated hands-on experience mapping HL7 standards (v2.x, v3) for orders, results, or clinical data., • 3 or more years utilizing modern API documentation standards (such as OpenAPI/Swagger) and API development tools (such as Postman)., • Experience with "Docs-as-Code" workflows and version control systems (e.g., Git, GitHub)., • Experience in healthcare interoperability in a diagnostic lab or clinical lab setting., • Deep knowledge of HL7 standards specifically applied to lab workflows (LOINC, SNOMED, and lab-to-EHR resulting)., • Knowledge of and practical experience with Fast Healthcare Interoperability Resources (FHIR) profiling and JSON data structures., • Experience working in an Agile/SAFe environment. Other Requirements: Knowledge: • In-depth knowledge of healthcare interoperability standards, data structures, and clinical vocabularies (HL7, FHIR, JSON, XML)., • Knowledge of data-mapping techniques and technical requirements-gathering frameworks., • Knowledge of API architecture styles (REST, SOAP) and security standards (OAuth 2.0). Exceptional written communication, editing, and content design skills, with an extreme attention to detail., • Deep technical proficiency and the ability to interview technical teams to extract crucial product mechanics., • Experience with process optimization, structured terminology management, and technical troubleshooting., • Strong collaboration and consensus-building skills.

Job Description Job Title - Technical Writer & Specifications Analyst Location - Secaucus, NJ(Remote) Buy Rate - $50/hr W2 Mandatory Skills - Technical Writer(US healthcare), Complete understanding of HL7 versions, and FHIR Job Summary The Senior Technical Writer & Specifications Analyst is a hybrid role responsible for performing technical business analysis including requirements gathering and data mapping and translating those requirements into high-quality, developer-facing API specification documentation. This individual owns the complete lifecycle of documentation for our integration and interoperability services, including orders and results services. Working directly with clinical, technical, product, and analysis teams, they will define data specifications, construct mapping sheets, and build clear, user-friendly documentation to help both internal consumer teams and external customers seamlessly integrate with Quest systems. The ideal candidate has deep expertise in healthcare standards (HL7 and FHIR) and a proven background in simplifying complex integration workflows. Key Responsibilities • Partner with technical, development, and product teams to gather, define, and document technical requirements for new and existing interoperability services., • Create and maintain comprehensive, interactive API specification documentation (including schemas, endpoints, headers, and error codes) specifically for orders and results services., • Perform detailed data mapping, interface specification design, and clinical data flow analysis (e.g., mapping HL7 segments/fields and FHIR profiles)., • Develop and maintain technical guides, quick-starts, step-by-step tutorials, and release notes for both internal developers and external customer IT teams., • Validate technical specifications by actively testing APIs (using tools like Postman or cURL) and reproducing integration workflows to ensure accurate documentation., • Implement and manage a "Docs-as-Code " workflow, utilizing version control and markdown formatting to streamline review cycles and updates., • Collaborate during Agile backlog grooming and sprint planning to proactively identify documentation and interface specification needs early in the product lifecycle., • Standardize content across integration portals to ensure consistency, clarity, and adherence to both industry interoperability standards and brand style guides., • Promote an environment that encourages collaboration, initiative, continuous improvement, learning, and the generation of innovative ideas and solutions. Skill Requirements, • 5 or more years of experience in technical writing, business systems analysis, or integration analysis, with progressive responsibilities in documenting APIs or clinical integrations., • 3 or more years of experience in healthcare interoperability, with a focus on electronic health records (EHRs) and clinical data exchange., • Demonstrated hands-on experience mapping HL7 standards (v2.x, v3) for orders, results, or clinical data., • 3 or more years utilizing modern API documentation standards (such as OpenAPI/Swagger) and API development tools (such as Postman)., • Experience with "Docs-as-Code " workflows and version control systems (e.g., Git, GitHub)., • Experience in healthcare interoperability in a diagnostic lab or clinical lab setting., • Deep knowledge of HL7 standards specifically applied to lab workflows (LOINC, SNOMED, and lab-to-EHR resulting)., • Knowledge of and practical experience with Fast Healthcare Interoperability Resources (FHIR) profiling and JSON data structures., • Experience working in an Agile/SAFe environment., • Other Requirements Knowledge: • In-depth knowledge of healthcare interoperability standards, data structures, and clinical vocabularies (HL7, FHIR, JSON, XML)., • Knowledge of data-mapping techniques and technical requirements-gathering frameworks., • Knowledge of API architecture styles (REST, SOAP) and security standards (OAuth 2.0). Skills: • Exceptional written communication, editing, and content design skills, with an extreme attention to detail., • Deep technical proficiency and the ability to interview technical teams to extract crucial product mechanics., • Experience with process optimization, structured terminology management, and technical troubleshooting., • Strong collaboration and consensus-building skills.

Job DescriptionJOB SUMMARY • The ideal candidate will be responsible creating, editing and maintain high-quality documentation that communicates complex technical information clearly and concisely to a variety of audiences. This role requires collaboration with subject matter experts, product managers, engineering team, and other stakeholders to ensure accurate and accessible content., • This is 6 Months contract to hire job position and could be based out out of Boston, MA or Jersey City, NJ., • Key Skills: Software development role, legacy financial institutions technology and API Integration architecture, Technical Writer, with a focus on API and ABI Documentation, Blockchain and Web3 technologies. Key Responsibilities:, • Provide expertise and guidance and best practices on product documentation set up for commercial purposes, • Review existing documentation related to product and applications and identify areas of improvement for our documentation strategy, • Work with UX team to optimize the setup of documentation on Resource Hub, • Work with Product, engineering and commercial teams to generate content and publish product requirements, operational flows, user and technical related material, • Establish standardized process and templates where possible for the efficient delivery of a consistent library of documentation for Ledger Scan, CMP and Factory to include the following (not limited):, • Product architecture diagram., • User Guide., • Production functional features., • APIs and End Points (where applicable)., • ABIs and Scripts (where applicable)., • Workflow Diagrams., • Infrastructure Requirements., • Deployment Diagrams., • Assist with content generation and production of documents as necessary., • Assist in creating content strategies and documentation plans to support product development., • Collaborate with cross-functional teams to understand end-user needs and incorporate feedback. Skills and Experience Required, • 5 years of experience as a Technical Writer, with a focus on API and ABI documentation, • 2 years of experience in a software development role, • Experience with legacy financial institutions technology and API integration architecture., • Experience with Blockchain and Web3 technologies., • Strong understanding of APIs, RESTful web services, and programming concepts, • Proficiency with various authoring, CMS, and task management tools, • Familiarity with API documentation tools, such as Swagger, Postman, or similar., • Proficiency with Confluence, JIRA, and JSON., • Basic diagramming skills using tools like draw.io, Miro or similar., • Experience using tech stacks like Python, MongoDB, CDC, and Kafka, • Experience working in a fast-paced, dynamic environment., • Strong time management skills., • Ability to thrive in an environment that grants you a lot of autonomy to explore creative solutions. Must have:, • 5 years of experience as a Technical Writer, with a focus on API and ABI documentation., • 2 years of experience in a software development role., • Experience with legacy financial institutions technology and API integration architecture., • Experience with Blockchain and Web3 technologies., • Strong understanding of APIs, RESTful web services, and programming concepts., • Proficiency with various authoring, CMS, and task management tools., • Familiarity with API documentation tools, such as Swagger, Postman, or similar., • Proficiency with Confluence, JIRA, and JSON., • Basic diagramming skills using tools like draw.io , Miro or similar., • Experience using tech stacks like Python, MongoDB, CDC, and Kafka, • Experience working in a fast-paced, dynamic environment., • Strong time management skills., • Ability to thrive in an environment that grants you a lot of autonomy to explore creative solutions

Job Description Position Overview: We are seeking a meticulous and experienced Technical Writer to join our team. The primary responsibility of this role will be to create and maintain department manuals within the company, ensuring clarity, accuracy, and compliance with internal standards. Additionally, the Technical Writer will collaborate closely with the Compliance Director to update and enhance compliance documents as necessary. Responsibilities: • Develop comprehensive department manuals that outline procedures, policies, and guidelines in clear and concise language., • Collaborate with department managers across various departments to gather information and ensure accuracy of content., • Update existing manuals on a regular basis to reflect changes in procedures, policies, and regulatory requirements., • Work closely with the Compliance Director to review and revise compliance documents, ensuring adherence to industry standards and legal requirements., • Ensure all documents are formatted, edited, and published according to company standards and branding guidelines., • Maintain a repository of all manuals and documents, ensuring version control and accessibility for all stakeholders., • Continuously improve documentation processes and standards based on feedback and industry best practices. Qualifications: • Bachelor’s degree in Technical Writing, English, Communications, or a related field., • Proven experience as a Technical Writer or similar role, • Excellent writing, editing, and proofreading skills with a keen eye for detail., • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and experience with document management software., • Ability to work independently and manage multiple projects simultaneously under tight deadlines., • Strong interpersonal skills and the ability to collaborate effectively with cross-functional teams., • Bilingual in Korean and English Benefits: • Comprehensive health benefits package (medical, dental, vision)., • 401(k) retirement savings plan with company match., • Paid time off (vacation, sick leave, and holidays)., • Gym Reimbursement, • Life Insurance, • Employee Referral Program

Job Description Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transforms patients’ lives. Through our unique approach to gene science based on Nobel Prize-winning technology, we are moving forward rapidly to bring innovative therapies to market. At Lexicon, our passion and dedication is driven by the patients for whom we work. Lexicon employees are inspired by the idea that their work can improve patients' lives and we know that our employees are essential to the success of our mission. Every day they bring their passion, talents and dedication to an engaging environment where they are rewarded with opportunities to realize their potential and ultimately impact the lives of patients. We are dedicated to making Lexicon a great place to work by providing employees with the benefits, services, and programs as part of our total rewards package. Join our journey and be a part of our multitalented team and make a difference in patients’ lives! Lexicon Pharmaceuticals is currently recruiting for a collaborative, agile, results focused Senior Medical Writer to join our team in either in Bridgewater, New Jersey, The Woodlands, Texas, or remotely. Job Summary: The Senior Medical Writer will support the Research and Development Organization and the Quality and Regulatory Organization by facilitating the production of accurate, concise, accessible, and compliant documents for Lexicon research, development and regulatory activities. They will serve as a company subject matter expert on processes and tools for organizing, writing, editing and reviewing research, development, quality and regulatory documents. Responsibilities include, but are not limited to: • Guiding and coordinating cross-functional collaborations with key company stakeholders to develop research, quality and regulatory documents, • Helping to integrate chemistry, manufacturing, non-clinical and clinical trial information and data into concise and compelling reports and summaries (conference presentations, abstracts, posters, and slides) and journal manuscript submissions, • Leading writing, editing, and cross functional review of clinical protocols, amendments, and clinical study reports, ensuring accuracy, clarity, completeness, and compliance with established formatting, content and style guidelines, • May serve in an oversight role in the assembly and/or QC of final study reports, • Overseeing external contractors including CROs in the authoring of Lexicon documents, including preparing concise and unambiguous requirements statements or SOWs, • Ensuring process consistency with Lexicon SOPs and applicable Lexicon standards for completeness, degree of detail, quality (including data accuracy) and style/formatting according to pre-agreed timelines, • Assisting in the development and maintenance of procedures and supporting documentation for the creation, review, and approval of documentation of Lexicon research activities, including, but not limited to, SOPs, templates, Word toolbars, work practices, best practices training guides and aids for Lexicon authors and reviewers, • Serving as the Protocol Review Committee (PRC) Coordinator, to ensure that all PRC-related materials are efficiently collected, reviewed, finalized, and retained according to Lexicon SOPs, • Serving as the Clinical Data Review Committee (CDRC) Coordinator, • Ensuring that all final versions of documents are filed in secure network locations, and, where needed, version controlled with correct access permissions and security, • Serving as a subject matter expert on processes and tools for organizing, writing, editing and reviewing research, development, quality and regulatory documents, • Maintaining, updating and providing training on the Lexicon Style Guide for authors and the Lexicon Reviewer Guide for reviewers, • Estimated Allocation of Effort:, • Authoring of documents: 40%, • Reviewing of documents: 40%, • Training: 10%, • Other: 10% Required Experience: • Bachelor’s Degree in a scientific/healthcare field in which writing is a major component is required, • AMWA membership and ELS certification is a plus, • Minimum of five (5) years of medical writing experience in a CRO, medical communications company, pharmaceutical company or other medical/scientific setting, • Knowledge of the drug development and approval processes in the U.S. is required, • Prior experience authoring publications, protocols, CSRs, Non-clinical reports and related documents; IND and NDA modules and summaries and other regulatory documents, • Experience with oversight of external Medical Writers and deliverables is required, • Skilled and adept with Microsoft Word, Microsoft SharePoint, Endnote, Adobe Acrobat For additional information about Lexicon and its programs, please visit www.lexpharma.com. Lexicon is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran. Lexicon Pharmaceuticals, Inc. is a drug-free workplace. Candidates are required to pass a drug test, background check and verification of credentials before beginning employment.

Job DescriptionDo you love using words to captivate, inform, and inspire action? Can you seamlessly adapt your writing style to different formats and audiences? How about a knack for the occasional pun? If so, we want to meet you! The Dog & Cat Business Unit within Central Garden & Pet is seeking a Content Writer Intern to join our Content Team in Neptune City, NJ. You’ll create content that elevates our brands and resonates with consumers across various touchpoints. This is an exciting opportunity to dive into the creative-meets-strategic world of content creation—crafting everything from website articles and social media posts to packaging copy, emails, press releases, and beyond. Ideally, you’re a wordsmith with demonstrated content creation and copyediting skills. You can easily pivot style and tone for the brand and channel, and you’re comfortable working both independently and in a team setting. You will report to the Associate Director, Content Business Strategy in the Creative Department. This position is based out of our Neptune City, Nj facility 5x a week. MEASURES OF SUCCESS: • Write original and engaging copy for a variety of platforms—websites, e-commerce, packaging, newsletters, social media, sell sheets, press releases, and more., • Adhere to style guidelines to create content in each brand’s unique voice, tone, and format., • Effectively manage multiple assignments to meet deadlines., • Regularly contribute fresh and creative content concepts/ideas., • Conduct competitive research to help enhance brands’ market presence., • Write and optimize website/e-commerce content for traditional SEO and emerging Answer Engine Optimization (AEO) and Generative Engine Optimization (GEO) best practices., • Integrate AI tools into your drafting and editing workflow to support, not replace, your own writing and editorial judgment as you move from first draft to final copy., • Stay curious about new AI tools and techniques, experimenting with what works best for different content types and sharing learnings with the team., • Conduct keyword research for search engine optimization on both search results and e-commerce platforms. IDEAL CANDIDATE ATTRIBUTES:, • Published writing samples or a link to an online portfolio are required for consideration, • 2-3 years of experience writing content either in-house or an agency setting, • Bachelor’s degree in English, Journalism, Communications, Marketing, or related field, • Proven writer and proofreader with professional written and verbal skills, • Ability to adapt tone and writing style based on medium and audience, • Can prioritize multiple types of projects in a fast-paced environment, • Familiarity with e-commerce product content, • Understanding of SEO/AEO/GEO best practices is preferred, • Experience with keyword research tools such as SEM Rush is preferred At Central Garden & Pet (NASDAQ: CENT and CENTA), we believe home is at the center of our lives, and our employees are driven by our purpose to nurture happy and healthy homes. Our company is made up of thousands of people across North America, with an emerging footprint across the U.K., Mexico, China, and Canada - all dedicated to helping gardens bloom bigger, pets live healthier, and communities grow stronger. We are united by our mission to lead the future of the garden and pet industries…one blade of grass and one wagging tail at a time. Visit our website at www.central.com to learn more. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, or any other characteristic protected by law.

Job Description Employment Type: Full-Time Location: On-site at our Newark HQ Hours: Monday–Thursday, 8AM – 5PM, Friday, 8AM – 1PM About the Role Fabuwood is seeking a Content Writer to bring the Fabuwood brand to life through clear, engaging, and on-brand copy. This role is responsible for writing content across all marketing touchpoints including email, blogs, social media, and web, making sure every word reflects Fabuwood's voice and supports our marketing goals. The Content Writer will report to the Brand Marketing Manager and work closely with graphic designers and the broader marketing team. Key Areas of Responsibility Email • Write copy for marketing emails, including campaigns, newsletters, product launches, and promotional sends to homeowners, dealers, and the design community., • Craft subject lines, preview text, and calls to action that drive opens, clicks, and engagement., • Partner with design and marketing teams to build email content that aligns with the campaign calendar., • Review email performance and use results to refine messaging and test new approaches. Blog • Plan, research, and write blog articles covering product features, design inspiration, industry trends, and home renovation topics., • Apply SEO best practices, including keyword research, headlines, meta descriptions, and internal linking., • Maintain the blog content calendar and keep a steady cadence of fresh content., • Repurpose blog content for use across email, social, and web. Social Media Copy • Write captions and copy for Fabuwood's social channels, tailored to each platform's audience and format., • Develop copy for organic posts, paid social ads, and campaign launches., • Collaborate with designers to pair copy with visuals that tell a cohesive story., • Stay current on social media trends and platform best practices. Web Copy • Write and update copy for the Fabuwood website, including product pages, landing pages, and campaign pages., • Translate complex product information into clear, simple language that consumers with little product knowledge can easily understand., • Prioritize clarity, useful information, and product understanding while maintaining engaging, brand-aligned messaging., • Optimize web copy for SEO, readability, and conversion., • Keep website content current, accurate, and consistent as products and campaigns change. Marketing Collateral • Write copy for print and digital marketing collateral, including brochures, catalogs, point-of-sale displays, sell sheets, and other sales and showroom materials., • Partner with designers to develop collateral that is visually compelling and aligned with brand standards., • Ensure product information and specifications in collateral are accurate and up to date., • Support dealers and the sales team with copy for materials used in showrooms and customer-facing settings. Brand Voice & Quality • Ensure all copy follows Fabuwood's brand guidelines, tone of voice, and messaging framework., • Edit and proofread content for accuracy, clarity, grammar, and consistency., • Follow established review and approval processes for all content before publishing. Collaboration & Research • Partner with the marketing team to support campaigns, product launches, and content initiatives., • Research industry trends, competitors, and product information to inform content., • Bring new content ideas and suggest improvements to existing content. Qualifications • 2+ years of experience in copywriting or content writing, ideally in marketing, home design, or a related industry., • A portfolio showing range across email, blog, social, and web copy., • Excellent writing, editing, and proofreading skills with a sharp eye for detail., • Working knowledge of SEO best practices., • Ability to adapt tone and style across channels and audiences while staying on-brand., • Strong organizational skills and the ability to manage multiple projects and deadlines., • Desire to research and understand industry trends to incorporate in writing, • Familiarity with email marketing platforms, CMS tools, and social media platforms is a plus.

Job DescriptionAbout ETS:ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 80 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL®, TOEIC®, GRE® and Praxis® tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, ACT solidifies our impact in higher Ed and Workskills while Edusoft enhances our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. The Product Management Lead is directly accountable for end-to-end management of major product line or major product line segment. This specific Lead Product Management position is for a technical writer for the NAEP project. Strong technical writing skills are essential for translating complex product and technical requirements into clear, accurate, and actionable documentation for technical and non-technical stakeholders. The Product Management Lead directly contributes to Product and SBU success and operates with full autonomy. Responsibilities End-to-End Product Mgmt & Delivery • Direct end-to-end execution of particular processe(s) associated with delivery of assigned product., • Direct work of FCEs to meet SLAs, • Extensive technical writing and maintain quality of deliverables to meet the standards. Contract/SLA Fullfillment • Work with FCEs to develop work plans and manage service level agreements. Define annual scope of work, timetable, work plan for assigned product/product segment., • Ensure that milestones are met, contractual obligations are fulfilled and delivery meets client expectations., • Ensure resolution of AD, statistical operation issues. Product Portfolio Mgmt • Oversee design and construction of assessments and perform quality checks, • Ensure appropriate application of research, test use, standards etc., • Facilitate and respond to internal audits, • Manage and/or launch new product concepts/extensions. Financial Mgmt. • Responsible for P&L (expense management, forecasting and monitoring budgets). Adhere to ethical standards and comply with the laws and regulations applicable to your job function Process Outputs Process Outputs and Deliverables (From the key responsibilities above, describe the most important process outputs of the role) • On-time and defect-free product releases, • Revenue, forecast and margin meet established targets, • Increased customer satisfaction, • Internal and external training materials, • Subject Matter Expertise on assigned product or product line, • Work plans, • Contractual deliverables and obligations fulfilled, • New Product launches, • Quality checks Criticality, Complexity and Interdependence • The Product Management Lead provides development and oversight of multiple functions necessary for the success of a major ETS product or product line., • This role entails moderate to high levels of risk, accountability and responsibility as the Product Manager leads development and implementation activities for major product segment or revenue product line., • Failure to deliver an on-time and budget, accurate product will delay organizational goals and incur significant monetary loss., • The Product Management Lead works across internal and external lines to determine a multi-functional approach and methodology for complex product management processes., • Stakeholders include senior management, Products and Services staff members, Finance and Marketing departments, Business Development, IT, Assessment Development, Research and Statistical Analysis, vendors, customers and channel partners., • Senior management is dependent on the Product Management Lead for complex project and process management for major products (upstream)., • Clients are dependent on the Product Manager Lead for major product releases and as a point of contact (downstream). Required Skills • Leadership, • Business Acumen, • Written Communication, • Presentation Skills, • Assessment, • Financial Literacy, • Product Knowledge, • Project Management, • Meeting Managment and Facilitation, • Client Relations, • Marketing Education, Certifications, or Special Licenses: • Advanced degree in Education, Education Measurement, Product Content Area or a related field strongly preferred., • A relevant combination of education and experience is preferred. Relevant Years of Experience Required: • 7 years experience in complex project management and/or process management is critical. Other Requirements (Specialized skill sets, behavioral/technical): • General knowledge of platform and assessment development product development and psychometric processes is required; deeper knowledge one of three is desirable. Must complete a government security clearance investigation and fingerprint check. Eligibility requirements include U.S. citizenship. #LI-NK1 ETS is mission driven and action oriented • We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning., • We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. Â In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth!, • As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. Â At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you!, • The base salary range advertised represents the low and high end of the anticipated salary range for this position. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. The base pay is only one aspect of the Total Rewards Package that will be offered to the successful candidate. ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.

Job Description At Thorlabs, we design and manufacture components, instruments, and systems that transform the world by identifying, enabling, and accelerating key photonics (i.e., light-based) technologies. Backed by a dedicated workforce of more than 3,000 employees worldwide, Thorlabs contributes to cutting-edge research and real-world innovation. Whether you're early in your career or bringing years of experience, you’ll find opportunities to grow, take ownership, and make meaningful contributions from day one. We know every employee brings unique talents and perspectives that fuel our success, and we seek driven individuals who are excited to make an impact in a fun, fast-moving culture. The Senior Science Writer role is responsible for strengthening Thorlabs’ position as a leading manufacturer of Photonics products through the creation of effective technical presentations, application images, videos, and other marketing collateral that inform and educate the photonics community about Thorlabs’ products/capabilities and their applications. Using photonics knowledge gained through extensive hands-on laboratory experience combined with knowledge gained through discussion with engineers, this role will define and drive the forward movement of the organization’s customer-centric marketing efforts. This role works closely with graphic artists to create content for the website or other marketing collateral. Although the position is based out of Newton, NJ; Lafayette, Colorado; or Rochester, New York, from time to time it may be required to undertake duties at other Thorlabs locations or to attend tradeshows. • Project Management: Plans, develops, and executes the successful and timely delivery of high-quality technical content in support of New Product Introduction (NPI), website updates, product discontinuation/supersession, acquisitions, tradeshows, social media posts, video/animation projects, or other marketing collateral utilizing technical expertise combined with information gained from conversations with key stakeholders. Content submitted, regardless of subject complexity, should require minimal feedback when it comes to technical accuracy, completeness, and adherence to Thorlabs standards for layout., • Content Strategy: Ensures customers can make informed and efficient decisions on which product(s) best serve their needs amidst a portfolio of 20,000+ items, developing/implementing proposals for website (re)organization as needed, ensuring strong cross linkage across the website, incorporating search engine optimization tactics as appropriate, and ensuring all documentation is comprehensive and meets organizational standards., • Timely Updates: Consistently meets deadlines, producing technically accurate content that meets company standards all while handling multiple projects at different stages of production and at all levels of technical difficulty., • Communication: Guides graphics and digital marketing staff by clearly and effectively communicating desired outcomes to obtain the necessary images, videos, and animations for a successful presentation. Partners with business unit leaders, engineers, and subject matter experts, as appropriate, to gather information and ensure content accuracy. Communicates effectively to address issues and achieve desired outcomes., • Coaching/Mentorship: Able to coach junior team members and assist Editorial Content Strategists by reviewing updates to presentations created by other Science Writers to support NPI, product revisions, product feedback, and general website improvements, ensuring they follow Thorlabs’ standards and are technically sound. Independently conceives of and builds application examples and/or guides others in the construction of application examples that help customers understand how products are utilized within a lab environment., • Website Enhancements: Collaborates with the eCommerce Project Manager and marketing management to develop, test and implement tools (e.g., configurators) that are necessary for new product introduction or an improved customer buying experience., • Product Road Mapping: Participates in defining new products and/or product enhancement through participation in the internal product development forum., • Project Oversite: Leads projects or ad hoc teams as needed to meet business needs. Requirements Experience: • 5+ years of significant hands-on laboratory experience. Education: • Advanced degree in Physics, Optics, Lasers, or a closely related field or a bachelor’s degree plus 10 years of equivalent work experience. Specialized Knowledge and Skills: • Extensive laboratory experience and familiarity with photonics equipment., • Expertise in writing brand-consistent content that meets project goals and addresses user needs., • Strong Organizational and Planning Skills., • Great presentation and communication skills with the ability to understand the audience, to structure effective presentations, and distill key messages to effectively inform and persuade., • Ability to flourish with minimal guidance, in a dynamic, fast-changing environment, and to be proactive in times of ambiguity., • Excellent writing and presentation skills in English., • Ability to Multitask, Be Detail Oriented, and to Solve Problems, All While Under Tight Time Constraints., • Familiarity with SEO best practices. The estimated pay range for this role is $ 75,000 - $ 94,300 annually Thorlabs values its diverse environment and is proud to be an Equal Employment Opportunity/Affirmative Action employer. All qualified individuals will receive consideration for employment without regard to race, color, religion, gender, gender identify or expression, sexual orientation, national origin, genetics, disability, age or veteran status. Job descriptions are not intended as and do not create employment contracts. The organization maintains its status as an at-will employer. Employees can be terminated for any reason not prohibited by law. Benefits Thorlabs offers a complete benefits package that includes medical, dental and vision insurance, company paid life insurance, a generous PTO package, a 401(k) plan, and tuition reimbursement just to name a few.

Job Description THE COMPANY Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies. We advise on learning strategies and create the right experiences, including online study, virtual, in-person and hybrid workshops, reference resources, sales/corporate training events, and more. We also work strategically with clients to create medical education for and outreach to healthcare professionals (HCPs) so they can make informed decisions in their practices. As we are rapidly expanding and have an opportunity for a Scientific Writer/Content Specialist to join our team in Princeton, New Jersey. THE LOCATION This position requires work to be performed from our Princeton, NJ offices. THE WORK Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several different styles of training, primarily interactive media such as eLearning, instructor-led courses/workshops, videos, and print resources; and (2) medical communications activities such as advisory boards, symposia, and speaker slide decks For these materials, within the constraints of our/clients’ guidelines, you will: • Review client’s goals and strategy, • When appropriate, develop learning objectives, appropriate for the audience (role, level), • Create or select content (medical, legal, regulatory) that is accurate and flows logically, • Apply general instructional design techniques, including (where appropriate) creating exercises and assessments, feedback, virtual meeting needs, ensuring materials are suitable for later translation, etc., • Obtain and incorporate input and insights from clients, subject matter experts (SMEs), key opinion leaders (KOLs), and other team members, • Reference the content according to the established referencing standards, • Provide additional strategic support, such as attending and developing executive summaries from advisory board meetings Content spans life science company requirements, from medical to policy and procedures, compliance, etc. You’ll be working primarily in Microsoft Word and Microsoft PowerPoint, often inside existing templates. You will work closely with internal team members to ensure successful project completion and delivery. You’ll also collaborate with your colleagues in the creative and development departments to help deliver the content in a way that is most impactful for the learner. This may involve a casual conversation or a brainstorming session to generate new ideas for presenting the information. There will likely be opportunities for additional work in curriculum design, audit and gap analysis, content creation for marketing collateral, as well as learning strategy, as the workload presents, and your capacity/interest aligns. As our work is collaborative, it will be necessary to work from our Princeton, NJ office, with some flexibility. THE CANDIDATE You have a degree or minor in a scientific discipline. You are proficient in PowerPoint and Word, with excellent writing and editorial skills - an English degree or minor is a plus. You are well-organized, with strong attention to detail. You have good presentation, communication, and interpersonal skills. You should have the capacity to: • Work in a fast-paced environment, pivoting to the highest priority or client need, • Bring creative ideas to the presentation and delivery of content, • Faithfully execute written and verbal instructions and seek clarification, when needed, • Work within established timelines and our clients’ regulated environments, • Attend project and client meetings, sometimes presenting your work, • Consider or explore the needs and perspective of your audience, • Speak your mind if you feel a project or process can be improved, • Learn new things and cultivate your capabilities as the workload may dictate THE FIT We are more interested in finding the right talent and attitude than the exact match to a list of skills and qualifications. We’re looking for someone that is excited and motivated to learn new things in creating learning/training/medical communications resources in scientific, compliance, and regulatory areas. BENEFITS • Retirement Plan Matching, • Medical Insurance, • Dental Insurance, • Vision Insurance, • Disability Insurance, • Paid Time Off Powered by JazzHR 2cmcHDJaIx

Job Description Marketing Content Writer Lakewood, NJ $65,000–$90,000 DOE 9:00 – 3:00 PM Position Overview We are seeking a creative and talented Marketing Content Writer to develop engaging, high-quality content across multiple marketing channels. This role is ideal for someone with strong writing skills, creativity, and the ability to craft compelling content that aligns with the organization's brand and marketing goals. Key Responsibilities Write and create engaging content for email marketing campaigns, advertisements, and social media posts. Develop compelling marketing copy that drives engagement and supports promotional initiatives. Create content for various marketing materials and campaigns. Collaborate with the marketing team to ensure consistent messaging and branding across all platforms. Brainstorm creative content ideas and contribute to marketing strategies. Manage multiple content projects while meeting deadlines. Qualifications Minimum 2 years of professional content writing, copywriting, or marketing content creation experience. Excellent writing, editing, and proofreading skills. Proven experience creating content for email campaigns, advertisements, and social media. Strong creativity and ability to adapt writing styles for different audiences and platforms. Highly organized, detail-oriented, and able to manage multiple projects. Ability to work collaboratively in a fast-paced marketing environment. To Apply: Send your resume to ahuva@maiplacement.com

Job Description Story so far In 2017, INEOS Chairman Sir Jim Ratcliffe, a British car enthusiast and experienced adventurer, identified a gap in the market for an uncompromising 4X4 engineered for modern day compliance and reliability. INEOS Automotive Limited was formed and a senior team of automotive professionals assembled to bring the vision to reality with a fresh perspective of 4X4 development and manufacturing. In 2022 the INEOS Grenadier was launched: a truly global 4X4 built from the ground up that combines rugged British spirit and design with German engineering rigour. The Grenadier provides best-in-class off-road capability, durability, and reliability with the modern comfort and refinement customers expect wherever they are in the world. In 2023 a double-cab pick-up variant of the Grenadier was launched called the Quartermaster. INEOS Automotive is a subsidiary of INEOS, a leading manufacturer of petrochemicals, specialty chemicals and oil products. It employs 24,500 people across 29 businesses, with a production network spanning 154 sites in 27 countries. From paints to plastics, textiles to technology, medicines to mobile phones, materials manufactured by INEOS enhance almost every aspect of modern life. In 2025, INEOS had sales of $55bn. To find out more about INEOS Automotive, visit www.ineosgrenadier.com. People and Culture Easy never changed anything. Not in manufacturing, science, engineering or energy - and certainly not elite sport. At INEOS we tackle every challenge head-on, and we help extraordinary athletes achieve extraordinary things. When it comes to making positive change, we know nothing gets done without grit, rigour and humour. Our Automotive team consist of around 1500 employees, 10 locations and 44 nationalities, we're an international team working together to challenge the ordinary. If this sounds like you, let's talk. Your role: The Senior Press Officer, Americas is a key role within the INEOS Automotive Global marketing team. The primary focus of this position is to develop and execute strategic media relations programs that increase the visibility of the INEOS Grenadier brand and product portfolio and build positive public perception across the US and Canada. Working closely with local and global marketing, communications, media, and leadership teams, you will shape and communicate the INEOS Automotive brand story, establish strong relationships with influential journalists and content creators, and positively position our vehicles with new-car shoppers. Responsibilities include (but not limited to): • Media Relations: Build strong relationships with automotive, lifestyle and business journalists, content creators and influencers., • PR Campaigns: Develop and deliver media strategies supporting key business priorities, product launches and brand activity., • Media Coverage: Proactively identify opportunities and secure high-quality coverage across print, broadcast and digital media., • Content & Storytelling: Create engaging press releases, media materials, briefings and stories that bring the INEOS Automotive brand to life., • Press Fleet: Manage the press fleet strategy, vehicle loans and handovers to maximise media opportunities and fleet utilisation., • Agency Management: Lead our Americas PR agency, setting clear briefs and ensuring effective delivery., • Media Enquiries: Manage incoming media requests and coordinate interviews with senior leaders and spokespeople., • Monitoring & Measurement: Track coverage and media sentiment and use insights to measure and improve PR activity., • Events & Partnerships: Represent INEOS Automotive at relevant media and industry events and support product placement and brand integration opportunities., • Cross-Functional Collaboration: Work closely with regional and global teams to ensure clear and consistent communications., • Crisis Communications: Support the development and delivery of crisis communications plans when required. Requirements What we are looking for: • Education: Bachelor’s degree in Communications, Journalism, Public Relations, or a related field., • Experience: A minimum of 8 years’ experience in public relations or media relations, ideally with a strong focus on the automotive industry., • Media Track Record: Proven success in securing high-quality coverage across major automotive, lifestyle, business, and consumer publications., • Media Network: An established network of relevant media contacts across the automotive and lifestyle sectors., • Communication Skills: An excellent writer and storyteller who can turn complex information into clear, engaging content., • Relationship Management: Strong interpersonal skills with the ability to build credible, long-term relationships with journalists, content creators, agencies, executives, and internal stakeholders., • Agency Collaboration: Demonstrated experience briefing, collaborating with, and managing external PR agency partners., • Project Management: Strong organizational and project management capabilities, with the ability to manage multiple priorities and deadlines., • Media Monitoring: Experience using media monitoring, measurement, and analysis tools to evaluate communications performance., • Location & Travel: This is an office-based position located in Montvale, New Jersey, requiring occasional travel across the Americas. Desirable: • Work Style: A proactive, creative, and collaborative approach, with the ability to work independently and thrive within a fast-paced, evolving environment., • Additional Experience: Experience within a start-up, franchise, social media, digital marketing, or off-road automotive environment would be advantageous. If the role sounds of interest and you want to learn more, please apply. If your application is successful one of our team members will be in touch to arrange an initial conversation!

Job DescriptionNDI Engineering Company is seeking an experienced and highly motivated Proposal Writer to join our Business Development and Capture team. The ideal candidate will possess a strong understanding of federal government proposal development processes, particularly within the Department of Defense (DoD) market. This role is responsible for developing compelling, compliant, and persuasive proposal content that effectively communicates our technical capabilities, management approach, and value proposition. The Proposal Writer will collaborate closely with capture managers, subject matter experts, program managers, and executive leadership to develop winning proposals in response to federal solicitations. Our Proposal Writer is responsible for developing, writing, and submitting compelling and compliant proposals in response to government solicitations (e.g., Requests for Proposals or RFPs). The writer works within our internal teams, subject matter experts (SMEs), and business development staff to produce high-quality, persuasive documents that meet strict deadlines and complex regulatory requirements. Key Responsibilities: • Analysis and planning: Analyze government solicitations (RFPs, RFQs, etc.) and related documents to understand requirements, evaluation criteria, and deadlines. Develop proposal outlines, compliance matrices, and writing plans., • Content development: Develop/write and edit proposal volumes and sections, including technical, management, past performance, staffing, and executive summaries. Synthesize complex information from multiple sources into a clear and compelling narrative., • Collaboration: Work with SMEs to gather information and translate technical concepts into persuasive, easy-to-understand language. Coordinate with the contracts and pricing teams to ensure proposal accuracy., • Compliance and quality control: Ensure proposals strictly adhere to all government regulations, including the Federal Acquisition Regulation (FAR). Perform final edits, proofreads, and quality control checks for grammar, consistency, and formatting., • Management and coordination: Manage proposal schedules and deliverables to meet all submission deadlines. Coordinate production, including final document formatting, printing, binding, and submission., • Content management: Maintain and update a library of reusable proposal content, templates, and graphics., • Post-submission activities: Participate in post-submission activities like addressing clarification questions and attending debrief meetings. Required Qualifications: • Education: A bachelor’s degree in communications, English, Business, or a related field is highly desired., • Formal Shipley Associates training or demonstrated experience applying Shipley proposal methodologies., • Experience: A minimum of 2–4 years of proven experience in federal government and/or defense contracting proposal writing, • Technical knowledge: Familiarity with government procurement processes and regulations (e.g., FAR and DFARS) is crucial., • Communication: Exceptional writing, editing, proofreading and verbal communication skills, with the ability to convey complex ideas clearly and persuasively., • Organizational skills: Strong project management and organizational skills to manage multiple priorities under tight deadlines. Ability to manage multiple proposals and deadlines simultaneously., • Software proficiency: Proficiency with Microsoft Office Suite (especially Word), • Detail-oriented: Meticulous attention to detail to ensure 100% compliance with all solicitation requirements. Preferred Qualifications • Experience supporting proposals for the Department of Defense, Navy, Army, Air Force, Space Force, or other federal agencies., • Familiarity with capture management and business development processes., • APMP or Shipley training/certification, • Knowledge of technical disciplines such as engineering, cybersecurity, IT services, logistics, training, or systems integration.Key Competencies, • Superior written and verbal communication skills, • Critical thinking and analytical ability, • Strong collaboration and interpersonal skills, • Compliance-focused mindset, • Ability to work effectively under tight deadlines, • Self-starter with strong initiative and accountabilitySalary Range: $65,000-$70,000 NDI Engineering Company is a privately-held small business consulting firm. NDI provides engineering and technical services to Government clients chartered with responsibility for the defense of our country. NDI offerings include naval architecture, marine, civil, structural, mechanical, and electrical engineering and design services. NDI has a ISO 9001:2008 Certified Quality System and was a prior recipient of the U.S. Small Business Administration Region II, Prime Contractor of the Year Award. NDI's corporate office is located in Thorofare, NJ with additional offices at the Naval Business Center, Philadelphia, PA, and Virginia Beach, VA. NDI Engineering Company is an Equal Opportunity Employer. This contractor and subcontractor shall abide by the requirements of 41 CFR §§ 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, or national origin. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. NDI Engineering Company is a privately-held small business consulting firm. NDI provides engineering and technical services to Government clients chartered with responsibility for the defense of our country. NDI offerings include naval architecture, marine, civil, structural, mechanical, and electrical engineering and design services. NDI has an ISO 9001:20015 Certified Quality System and was a prior recipient of the U.S. Small Business Administration Region II, Prime Contractor of the Year Award. NDI's corporate office is located in Thorofare, NJ with additional offices at the Naval Business Center, Philadelphia, PA, and Virginia Beach, VA. NDI Engineering Company is an Equal Opportunity Employer. This contractor and subcontractor shall abide by the requirements of 41 CFR §§ 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, or national origin. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Powered by JazzHR rP7vuCoESo

Job Title: Director Medical Writer Location: Plainsboro, NJ 08536 Duration: 6+ Months Requirements: • Advanced degree in medicine, pharmacy, life sciences, or a related discipline (e.g., MD, PharmD, PhD), with a strong foundation in clinical research, medical science, and safety data interpretation., • Minimum 10 years of relevant experience in pharmacovigilance, clinical safety, regulatory medical writing, or a related pharmaceutical/biotechnology field, including substantial experience independently authoring complex safety documents and leading cross-functional authoring for major submissions., • Demonstrated experience leading safety authoring for complex marketing authorization and post-approval submissions, including document strategy, scientific content, review, and timely delivery., • Proven ability to independently author and critically review key safety and regulatory deliverables, including DSURs, PSURs/PBRERs, PADERs/PAERs, Risk Management Plans, signal evaluations, health authority responses, Summaries of Clinical Safety, Clinical Overviews, Integrated Summaries of Safety, CSR safety sections, and patient narratives., • Demonstrated expertise in integrated safety assessments and benefit–risk evaluations, synthesizing clinical trial, post-marketing, literature, and other relevant evidence into scientifically sound conclusions and regulatory positions., • Experience translating safety findings into risk management measures, safety labeling, and health authority responses, while ensuring consistent scientific messaging across regulatory and pharmacovigilance deliverables., • Strong understanding of global health authority expectations, CTD safety content, and pharmacovigilance requirements, with experience supporting regulatory submissions and health authority interactions., • Strong scientific judgment and ability to interpret complex clinical and safety data, identify material findings and evidence gaps, reconcile conflicting evidence, communicate uncertainty, and develop clear, persuasive medical narratives and recommendations., • Proven ability to lead multiple concurrent deliverables and cross-functional reviews, manage dependencies and timelines, resolve content gaps, and maintain high standards for accuracy, traceability, consistency, and inspection readiness., • Excellent scientific writing, executive communication, and cross-functional leadership skills, with the ability to influence senior stakeholders and collaborate effectively across Safety, Regulatory Affairs, Clinical Development, Biostatistics, Medical Writing, and other relevant functions. Experience developing authoring standards, templates, SOPs, training, and process improvements is also expected., • Oncology development and submission experience preferred, including familiarity with complex treatment settings, combination therapies, and interpretation of safety findings in patients with advanced disease and significant comorbidities Expertly prepare (or oversee the work of others), edit, finalize and contribute to the strategic direction of complex clinical and regulatory documents, including clinical trial protocols/amendments, investigator’s brochures, clinical study reports, PIPs, Health Authority briefing packages, Health Authority responses, and clinical CTD submission document Support in development, implementation, and execution of Medical Writing strategy in line with organizational strategy Serve as compound lead writer and medical writing representative on cross-functional study teams and provide advanced knowledge and guidance on document strategy and content, timelines, and resource needs to ensure timely completion of tasks with desired quality Responsibilities: The manager is looking to have someone start this assignment after the new year. He is open to having someone start in December if the timeline works out. REQ start date will be updated as needed. The Role: This role, Aggregate Safety Report (ASR) Project Management and Pharmacovigilance Medical Writer, leads the planning, project management, and scientific authoring of aggregate safety reports and other pharmacovigilance deliverables. It integrates and evaluates safety evidence to develop scientifically sound conclusions, ensures consistent safety messaging, and drives timely, high-quality, inspection-ready deliverables through cross-functional collaboration and continuous process improvement. Expertly prepare (or oversee the work of others), edit, finalize and contribute to the strategic direction of complex clinical and regulatory documents, including clinical trial protocols/amendments, investigator’s brochures, clinical study reports, PIPs, Health Authority briefing packages, Health Authority responses, and clinical CTD submission document Support in development, implementation, and execution of Medical Writing strategy in line with organizational strategy Serve as compound lead writer and medical writing representative on cross-functional study teams and provide advanced knowledge and guidance on document strategy and content, timelines, and resource needs to ensure timely completion of tasks with desired quality As required, oversee aspects of medical writing portfolio, including maintaining long-range forecast for Medical Writing needs Oversee medical writing activities and clearly establish expectations/responsibilities with partners/CROs/vendors Lead a submission team of Medical Writers providing vision, coaching, and oversight of deliverables Lead development and review of standard processes and templates for continuous process improvement and maintaining high quality and standards, and drive knowledge sharing sessions for cross-company initiatives Represent the Medical Writing team in forums (e.g. project boards, global development teams, operational committees, steering committees with partners, clinical management team, protocol review committee, regulatory submission teams).

Job Title: Communications Coordinator Location: Bridgewater, NJ Type of Employment: Temporary, 6 months In Office/Hybrid/Remote: Hybrid, 2 days a week in office Hourly - $25/hr Job Summary: A pharmaceutical organization in Bridgewater, NJ is seeking to hire a temporary Communications Coordinator to support a variety of internal and external communication initiatives. This position will assist with employee communications, corporate content, social media, communications projects, and reporting while working closely with teams throughout the organization. The ideal candidate is a strong writer with excellent organizational skills, attention to detail, and the ability to manage multiple projects and deadlines. This is a great opportunity for someone early in their communications career who is interested in gaining experience within the pharmaceutical, biotechnology, healthcare, or another highly regulated industry. If this opportunity aligns with your background and career goals, please apply for consideration. Responsibilities: • Assist with writing, editing, and distributing internal communications, including employee announcements, newsletters, leadership messages, intranet updates, event materials, and company-wide communications, • Manage communication calendars and help coordinate deadlines, review processes, approvals, and distribution schedules, • Turn business-related or technical information into clear and engaging content for employees and other audiences, • Provide communications and logistical support for company meetings, employee events, and engagement activities, • Maintain communication templates, internal resources, contact lists, content libraries, and archived materials, • Work with departments across the organization to gather information and ensure messaging remains accurate and consistent, • Assist with external communications, including website content, social media posts, presentations, fact sheets, press materials, and approved company announcements, • Help manage the corporate social media calendar, including drafting content, coordinating approvals, scheduling posts, monitoring activity, and tracking results, • Monitor designated communication and media inboxes, document inquiries, and direct requests to the appropriate team members, • Research industry developments, relevant media coverage, communication trends, and stakeholder topics, • Maintain media contacts, company background information, approved messaging, images, and other communication resources, • Review materials for grammar, accuracy, formatting, brand consistency, and overall quality, • Coordinate communication projects through the various stages of development, review, approval, distribution, and reporting, • Maintain project trackers, editorial calendars, status updates, and follow-up items, • Coordinate necessary reviews with internal departments such as Legal, Compliance, Human Resources, Regulatory/Medical, and other key stakeholders, • Collect engagement and communications data and assist with preparing reports on reach, performance, and other relevant metrics, • Look for ways to improve communication processes, content organization, and audience engagement, • Assist with additional communications projects and initiatives as needed Required Experience: • Bachelor’s degree in Communications, Public Relations, Journalism, Marketing, English, Business, or a related field, or an equivalent combination of education and relevant experience, • Previous communications experience gained through employment, internships, academic programs, volunteer work, or similar activities, • Strong written and verbal communication skills with the ability to create clear, concise content for different audiences, • Excellent proofreading, organizational, and attention-to-detail skills, • Ability to balance multiple assignments, shifting priorities, and deadlines in a fast-paced environment, • Strong judgment and a commitment to professionalism, confidentiality, and accuracy, • Comfortable collaborating with employees and stakeholders across different departments and levels of an organization, • Proficiency with Microsoft 365, including Word, Excel, PowerPoint, Outlook, and Teams, • Comfortable learning new content management systems, communication platforms, approval tools, and reporting technologies, • Interest in corporate communications and the ability to make complex or technical topics easier for different audiences to understand Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.lhh.com/us/en/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: • The California Fair Chance Act, • Los Angeles City Fair Chance Ordinance, • Los Angeles County Fair Chance Ordinance for Employers, • San Francisco Fair Chance Ordinance

Medical Director – Continuing Medical Education (CME) Remote | Full-Time | 10–15% Travel This is an excellent opportunity for an experienced clinical leader who enjoys translating complex scientific information into engaging educational content while collaborating with cross-functional teams and nationally recognized faculty. This position offers significant flexibility, a collaborative culture, and the opportunity to make a meaningful impact on healthcare education. Position Summary The Medical Director serves as the scientific and clinical lead for accredited continuing medical education (CME) initiatives. This individual will oversee the clinical quality, educational integrity, and strategic development of a diverse portfolio of educational programs across multiple therapeutic areas. The ideal candidate combines strong clinical knowledge with experience managing educational projects, collaborating with faculty, and ensuring compliance with accreditation standards. Responsibilities • Lead the scientific strategy and clinical development of accredited educational initiatives., • Translate emerging clinical research into engaging educational programs for healthcare professionals., • Partner with medical writers, educational planners, project managers, and commercial teams throughout program development., • Collaborate with key opinion leaders and faculty to develop evidence-based educational content., • Review presentations, educational materials, manuscripts, and supporting resources for scientific accuracy and clinical relevance., • Ensure programs meet accreditation requirements and industry compliance standards., • Develop learning objectives, educational outcomes, assessment strategies, and supporting materials., • Manage multiple educational projects while maintaining timelines and quality expectations., • Participate in faculty planning meetings and provide scientific guidance throughout project execution., • Oversee content quality assurance and final scientific review before program launch., • Attend selected live and virtual educational programs to support successful execution., • Build strong working relationships with internal teams, external experts, and educational partners. Qualifications • 5+ years of experience within Continuing Medical Education (CME), Medical Communications, Medical Affairs, or healthcare education., • Experience leading grant-funded educational initiatives from concept through execution., • Advanced scientific or clinical degree preferred (PharmD, MD, PhD, DO, MPH, or similar)., • Strong understanding of ACCME guidelines, educational compliance, and pharmaceutical industry standards., • Demonstrated ability to interpret complex clinical data across multiple therapeutic areas., • Experience working with physician faculty and key opinion leaders., • Excellent project management and organizational skills., • Strong written, verbal, and presentation abilities., • Ability to manage multiple priorities in a fast-paced remote environment., • Proficiency with Microsoft Office and common collaboration platforms. Preferred Background Candidates with experience in one or more of the following are especially encouraged to apply: • Continuing Medical Education (CME), • Medical Communications, • Medical Affairs, • Pharmaceutical Industry, • Biotechnology, • Medical Device, • Scientific Publications, • Clinical Education, • Healthcare Professional Education LinkedIn Search Keywords Medical Director • Continuing Medical Education • CME • Medical Communications • Medical Affairs • Medical Education • Scientific Director • Medical Writer • Healthcare Education • Clinical Education • Pharmaceutical • Biotechnology • Medical Device • PharmD • MD • PhD • ACCME • Grant-Funded Education • Clinical Research • Medical Affairs • Healthcare Professionals

Plainsboro, NJ - Hybrid (onsite 2-3 days per week) 6 Month Initial Contract - Potential for Extension Pay: $95-$105/hr The Senior Manager, GDS&PV Medical Writer is responsible for contributing to the medical writing portfolio within the clinical and regulatory areas. This includes authoring and contributing to the authoring of 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. The Senior Manager, GDS&PV Medical Writer participates in the development of templates and the establishment of medical writing processes and standards to ensure the quality and timeliness of regulatory filings and clinical documentation, in accordance with relevant regulatory guidelines and requirements. The Senior Manager proactively engages in departmental activities and lessons learned to share insights, lead various initiatives, and contribute to supporting a global organization. Responsibilities: Document Creation and Review • Independently author and review clinical and regulatory documents, including clinical trial protocols, amendments, and reports., • Prepare and review investigator’s brochures, clinical overviews, and summaries in CTD/eCTD format for regulatory submissions., • Draft and edit Health Authority briefing books, responses, and publications (abstracts, posters, slide presentations, and manuscripts for scientific journals). Team Leadership and Collaboration:, • Represent medical writing on internal teams such as the Clinical Trial Team, protocol review committee, and regulatory submission teams., • Lead or participate in submission team activities., • Facilitate team participation in document preparation, including scheduling meetings, developing timelines, and managing document reviews and decisions. Process Development: • Lead or participate in the development and review of standard processes and templates., • Support ongoing improvements in cross-functional and global collaboration, sharing best practices and knowledge., • Maintain current knowledge and competencies within relevant therapeutic and professional areas., • Contribute to knowledge sharing, skill-building, and good collaboration with stakeholders and colleagues. Regulatory and Quality Adherence: • Maintain up-to-date knowledge of relevant regulatory guidelines and requirements., • Adhere to guidelines, SOPs, practices, and technical standards in all aspects of work Qualifications: Independently prepare, edit, and finalize complex clinical and regulatory documents including clinical trial protocols/amendments, investigator’s brochures, and clinical study reports Independently draft and edit Health Authority briefing packages, Health Authority responses, and clinical CTD submission documents Serve as compound lead writer and medical writing representative on cross-functional study teams and provide guidance on document strategy and content, timelines, and resource needs to ensure timely completion of tasks with desired quality Manage smooth and effective document management from start to finish (i.e., from template to a final approved version) for a project/ trial Actively drive development of templates and establishment of medical writing processes and standards Recommend and lead process improvement initiatives and actively participate in inter-and intra-departmental knowledge sharing sessions Requirements: • Approximately 6–8+ years of relevant medical writing experience within the pharmaceutical or biotechnology industry, including experience independently leading complex clinical and regulatory documents., • Demonstrated experience authoring and investigator’s brochures, clinical summaries/overviews, briefing documents, and Health Authority responses., • Strong knowledge of clinical development, regulatory submission requirements, CTD/eCTD structure, ICH guidelines, and applicable global regulatory requirements., • Experience leading medical writing activities for regulatory submissions, including document planning, cross-functional reviews, timeline management, and resolution of complex reviewer comments., • Proven ability to interpret and communicate complex clinical and scientific data clearly, accurately, and consistently for regulatory and scientific audiences., • Strong project management, communication, and cross-functional collaboration skills, with the ability to represent Medical Writing on clinical development and regulatory teams and manage multiple priorities and timelines., • Experience contributing to medical writing standards, templates, processes, and continuous improvement initiatives, with a demonstrated commitment to quality, knowledge sharing, and development of best practices

AllSTEM Connections is seeking a Director, Aggregate Safety Reporting & Pharmacovigilance Medical Writing to work hybrid onsite in Plainsboro, NJ. This is a six-month contract position. Possible extension/temp-to-hire. Hourly rate is up to $140/hour. SUMMARY: This role, Aggregate Safety Report (ASR) Project Management and Pharmacovigilance Medical Writer, leads the planning, project management, scientific authoring, and delivery of aggregate safety reports and other pharmacovigilance-related regulatory documents. The position requires advanced scientific writing expertise, strong project management capabilities, and the ability to integrate and critically evaluate complex safety evidence to develop scientifically sound conclusions and consistent regulatory messaging. The individual will lead cross-functional authoring activities, manage document timelines and reviews, ensure high-quality and inspection-ready deliverables, and drive continuous improvement of medical writing processes. RESPONSIBILITIES • Lead the planning, project management, and delivery of aggregate safety reports and other pharmacovigilance documents, including DSURs, PSURs/PBRERs, PADERs/PAERs, Risk Management Plans, signal evaluation reports, and safety topic assessments., • Independently author complete documents or substantive sections of complex safety and regulatory deliverables, taking ownership from initial evidence review and document strategy through finalization and approval., • Integrate and critically evaluate safety evidence from clinical trials, spontaneous reports, published literature, nonclinical studies, and other relevant sources to characterize safety findings, assess clinical significance, and determine implications for the product safety profile., • Develop integrated safety assessments and benefit-risk evaluations, addressing temporal relationships, alternative etiologies, confounding factors, class effects, risk factors, data limitations, and areas of uncertainty., • Translate complex medical and scientific concepts, including disease biology, mechanisms of action, adverse event pathophysiology, and potential causal relationships, into clear, accurate, and scientifically balanced regulatory narratives., • Develop document strategies, structures, key scientific messages, and evidence-based conclusions, ensuring appropriate medical and cross-functional alignment and consistency across pharmacovigilance and regulatory deliverables., • Lead project management activities for aggregate safety reporting and other pharmacovigilance deliverables, including reporting calendars, timelines, milestones, resource planning, cross-functional reviews, approvals, and submission readiness., • Proactively identify project risks, bottlenecks, content gaps, and conflicting reviewer feedback, driving resolution while maintaining scientific accuracy, consistency, traceability, and inspection readiness., • Collaborate with Safety Physicians, Safety Scientists, Regulatory Affairs, Clinical Development, Biostatistics, and other subject matter experts to resolve scientific questions and align source evidence, analyses, conclusions, and regulatory positions., • Prepare and review safety content for regulatory submissions, investigator's brochures, safety communications, health authority responses, governance materials, briefing documents, presentations, and internal or external safety inquiries., • Oversee medical writing activities performed by internal partners, CROs, and external vendors, establishing clear expectations, responsibilities, timelines, and quality standards., • Provide medical writing leadership and strategic guidance to cross-functional teams, including serving as a compound lead writer or medical writing representative on relevant development and submission teams., • Perform scientific and quality reviews to ensure medical accuracy, data consistency, appropriate referencing, traceability, and compliance with applicable regulatory requirements and internal standards., • Develop, maintain, and improve aggregate safety reporting and pharmacovigilance writing processes, including SOPs, templates, guidance documents, and training materials., • Identify and implement improvements in project management, evidence synthesis, document development, and review workflows to enhance efficiency, quality, consistency, and compliance., • Represent Medical Writing in relevant cross-functional governance forums, project teams, regulatory submission teams, and operational committees. QUALIFICATIONS & REQUIREMENTS • Advanced degree in medicine, pharmacy, life sciences, or a related discipline (e.g., MD, PharmD, PhD), with a strong foundation in clinical research, medical science, and safety data interpretation., • Minimum 10 years of relevant experience in pharmacovigilance, clinical safety, regulatory medical writing, or a related pharmaceutical or biotechnology field., • Extensive experience independently authoring complex safety documents and leading cross-functional authoring activities for major regulatory submissions and post-approval requirements., • Demonstrated experience leading safety authoring for marketing authorization and post-approval submissions, including document strategy, scientific content development, review, and timely delivery., • Proven ability to independently author and critically review key safety and regulatory deliverables, including DSURs, PSURs/PBRERs, PADERs/PAERs, Risk Management Plans, signal evaluations, health authority responses, Summaries of Clinical Safety, Clinical Overviews, Integrated Summaries of Safety, CSR safety sections, and patient narratives., • Demonstrated expertise in integrated safety assessments and benefit-risk evaluations, synthesizing clinical trial, post-marketing, literature, and other relevant evidence into scientifically sound conclusions and regulatory positions., • Strong understanding of global health authority expectations, CTD safety content, and pharmacovigilance requirements, with experience supporting regulatory submissions and health authority interactions., • Strong scientific judgment and ability to interpret complex clinical and safety data, identify material findings and evidence gaps, reconcile conflicting evidence, communicate uncertainty, and develop clear, persuasive medical narratives and recommendations., • Proven ability to manage multiple concurrent deliverables and cross-functional reviews, including complex timelines, dependencies, resource requirements, and competing priorities., • Excellent scientific writing, critical review, executive communication, and cross-functional leadership skills, with the ability to influence senior stakeholders and collaborate across Safety, Regulatory Affairs, Clinical Development, Biostatistics, and Medical Writing., • Experience developing authoring standards, templates, SOPs, training programs, and process improvements to maintain consistent quality and regulatory compliance., • Oncology development and submission experience preferred, including familiarity with complex treatment settings, combination therapies, and interpretation of safety findings in patients with advanced disease and significant comorbidities. ADDITIONAL POSITION DETAILS • Work Arrangement: Hybrid, onsite 2–3 days per week., • Anticipated Start: Targeting a start after the new year, although a December start may be considered depending on candidate availability and project timing. Requisition start date may be adjusted accordingly., • Interview Process: Two rounds of interviews, including hiring manager and members of the team

Polaris Young Adult Christian Leadership Initiative Department: Marketing and Communications Employment status: Full-time, exempt; 5-year term grant-funded position (2027-2031) Hours per week: 35 Months per year: 12 Work schedule: Princeton Seminary office hours; occasional evening and weekend work based on network programming Reports to: Senior Director of Marketing and Communications Dotted-line relationship: Polaris Senior Program Director Salary Range: $81,000-88,000 (commensurate with experience) Submit Resumé and Cover Letter: communication@ptsem.edu Job Purpose The Communications and Content Manager leads communications and marketing implementation for the Polaris Young Adult Christian Leadership Initiative which supports 1) the Polaris Young Adult Leadership Network, 2) the Polaris Research Initiative, and 3) the Polaris Collaborative. As a member of Princeton Seminary’s Marketing and Communications team, this position builds awareness of the network’s direct programs with young adult leaders, supporting program enrollment and increasing participation in story-sharing initiatives. The manager translates program priorities into practical communications plans and develops content in collaboration with MarCom’s writing, social media, web, and photography staff and media production colleagues. The manager also cultivates a secondary audience of organization leaders invested in young adult faith and leadership by highlighting research and featured stories from the Polaris Research Initiative and the Polaris Collaborative. The position reports to the Senior Director of Marketing and Communications, who oversees communications strategy, work priorities, and performance. A dotted-line relationship with the Polaris Senior Program Director supports coordination around program goals, schedules, and participant needs. Essential Functions Marketing Strategy and Campaign Implementation | 30% • Develop and implement communications plans for Polaris programs and initiatives, defining target audiences, messages, channels, calls to action, timelines, and measures of success in consultation with the Senior Director and program leadership. Ensure priorities align with budget allocations. • Build campaigns that move audiences from awareness to inquiry, enrollment, and participation. Select and coordinate awareness campaigns, email nurture sequences, and conversion-focused outreach according to the goal and stage of audience engagement. • Work with MarCom colleagues and approved marketing partners to execute paid and organic campaigns, aligning advertisements, landing pages, email follow-up, and registration information. • Identify new media outlets, digital communities, distribution partners, and paid placements that can reach young adults and the people who influence their participation. Recommend opportunities based on audience relevance, cost, and likely results. • Apply participant feedback, market research, direct audience engagement, and professional judgment to refine messaging and test new approaches. Content Development and Story Sharing | 35% • Identify and develop stories that highlight young adult Christian leaders in diverse communities and contexts, connecting their experiences to Polaris’s purpose and opportunities for involvement. • Develop secondary audience of institutional and organizational leaders who champion young adults. Feature Polaris research and related interdisciplinary research about young adult faith formation and leadership development. Highlight exemplary Polaris Collaborative organizations along with stories featuring young adults. • Maintain an editorial calendar that coordinates stories, program promotion, and ongoing network communications across video, social media, web, email, and newsletters. • Write and edit audience-focused copy, develop creative briefs, and gather interviews, background information, and other materials needed for production. • Collaborate with MarCom’s writer, social media staff, web producer, photographer, and media production colleagues to develop and adapt content for each channel. Coordinate contributions and reviews through established team workflows and agreed timelines. • Plan distribution and reuse of stories across Polaris and Seminary channels, working with channel owners to identify appropriate placements and connect content to clear audience actions. • Ensure content is accurate, accessible, consistent with Seminary and Polaris brand standards, and appropriate for the audience. Coordinate participant permissions and approvals as needed. • Coordinate external creative vendors when specialized expertise or additional capacity is needed, with approval from the Senior Director and within established budgets. Program Partnership and Audience Relationships | 20% • Meet regularly with Polaris program directors to understand upcoming offerings, enrollment goals, story-sharing priorities, and emerging communications needs. • Translate program needs into actionable briefs for MarCom, clarifying audiences, deliverables, deadlines, and decisions required. Develop feasible plans with colleagues and communicate agreed priorities and progress to program leadership. • Build and sustain relationships with participants, alumni, Christian leaders, creators, and community partners who can contribute stories, inform outreach, or introduce the network to new audiences. • Stay engaged with the interests, language, media habits, and communities of young adults, particularly those ages 23–32. Recognize differences within this audience and identify trusted voices and organizations that influence their decisions. • Surface opportunities that may not arrive through formal project requests, including emerging stories, relevant conversations, partnerships, and gaps in the participant experience. • Participate in relevant Polaris and MarCom meetings and attend Polaris gatherings as needed to support relationships, storytelling, and communications. Performance Measurement and Team Operations | 15% • Track campaign and content performance, including audience reach, engagement, inquiries, registrations, and enrollment, where applicable. Summarize findings and recommend specific adjustments. • Work with colleagues responsible for CRM and email systems to support audience segmentation, campaign tracking, and timely follow-up with prospective and current participants. • Maintain project information, content schedules, and campaign records in MarCom’s shared systems. Flag missing information, competing deadlines, and resource needs early. • Contribute to program and grant reporting by providing communications results, campaign summaries, and examples of network reach and participation. • Participate in departmental planning and relevant institutional initiatives, and perform other related duties assigned by the Senior Director of Marketing and Communications. Required Qualifications and Skills • Bachelor’s degree in marketing, communications, journalism, or a related field, or an equivalent combination of education and relevant experience. • A minimum of three years of marketing and communications experience, including hands-on implementation of integrated digital campaigns. • Experience marketing educational programs, membership networks, nonprofit initiatives, or leadership development opportunities. • Experience with Salesforce Marketing Cloud, WordPress, and Monday.com or comparable platforms. • Experience collaborating on video production, including interviewing, story development, and adapting video for digital channels. • Candidates must demonstrate work that connects content and outreach to audience growth, inquiries, registrations, or comparable outcomes. • Demonstrated success engaging young adult audiences, supported by current familiarity with their digital communities, cultural interests, media habits, and trusted sources of influence. • Strong writing, editing, storytelling, and creative briefing skills., • Practical knowledge of social media publishing and paid promotion, email marketing, website content, and campaign analytics. • Ability to interpret audience research and performance data while exercising sound editorial and marketing judgment, proposing ideas, and testing assumptions. • Strong relationship-building and listening skills; ability to work effectively with Christian leaders and audiences with varied theological, cultural, and professional backgrounds. • Demonstrated ability to collaborate across specialties, work within shared priorities, incorporate feedback, and carry projects from planning through delivery. • Experience using email marketing platforms, content management systems, CRM tools, and basic design tools. • Strong organization, attention to detail, and ability to manage multiple projects and meet deadlines. • Ability to maintain confidentiality, steward sensitive information, and exercise care when sharing participants’ stories. • Commitment to Princeton Seminary’s mission and to equity, inclusion, diversity, and antiracism. Physical and Environmental Demands • Remote/Hybrid flexibility., • Ability to be on campus to support key initiatives throughout the year.

Job Title: MedInfo Medical Writer Location: Titusville, NJ - on site 3x/week Contract Length: 1 Year Contract We are looking for a Medical Writer to join the Medical Information team with our pharmaceutical client. This person should have a PharmD, and will be responsible for medical writing, scientific content review, and content maintenance in support of Medical Information Content Strategy and Innovation (MI-CSI). - Creates and updates patient scientific responses, supports content management and quality assurance for payer digital content and innovative and digital healthcare professional (HCP) content, and provides backup support for global medical information escalations as needed. - Collaborates with internal scientific partners to deliver accurate, balanced, clearly written, and audience-appropriate content. - Strong medical writing, literature evaluation, and scientific review capabilities are the primary requirements for this role. - Experience with digital content platforms, design tools, or artificial intelligence (AI) is an additional asset. Must Haves: • Doctor of Pharmacy or equivalent advanced scientific or clinical degree, • 2 Years of Experience in Medical Writing, • Writing experience specific to Medical Information, strong familiarity with SRL's and SLD's, • Demonstrated experience writing and reviewing scientific or medical information content, conducting literature searches, and interpreting clinical evidence., • Experience collaborating with cross-functional scientific teams and managing multiple content assignments and deadlines. Strong medical writing and scientific research skills, with the ability to synthesize evidence and communicate accurately for different audiences, including patients., • Strong clinical and scientific judgment, attention to detail, and ability to identify and resolve content quality issues. Proficiency in Microsoft Word and working knowledge of PowerPoint and Excel; ability to learn the collaboration and content management tools needed for assigned work. Compensation: $50- $60 per hour Exact compensation may vary based on several factors, including skills, experience, and education.

Job Title: Digital Copywriter and Copy Editor, Marketing (consultant) Location: Weehawken, NJ 07086 (Hybrid) Hybrid: 3-4 days per week onsite Job type: Contract Role (W2) Are you ready to make an impact on a fast-paced, client-focused marketing team? As a digital copywriter and editor, you will play an important role in shaping our online presence and ensuring the accuracy and effectiveness of our digital content. But beyond copy writing, editing, and proofreading, you’re a strategic storyteller with a keen eye for SEO, generative engine optimization (GEO) and digital content nuances. If this sounds like you, this opportunity may be a great fit. What you’ll do: • Craft compelling digital content. Your words matter. You will develop engaging and search optimized content for our digital platforms. You will transform complex financial concepts into clear, digestible content that resonates with our target audiences. You’ll craft compelling content for websites, social media and e-mail campaigns promoting our solutions, thought leadership and events to drive client and Advisor conversations including:, • Responsive website/page design, wireframing content, • Social media and interactive ad units, • Mobile applications/platforms, • HTML e-mails, • Interactive and static infographics, • Interview, live action and motion graphic-animated videos, • Copy editing and proofreading. We’ll count on you to be a perfectionist and help polish content until it gleams. That requires understanding our brand voice and tone as well as spotting and correcting all grammatical errors, typos and inconsistencies., • Editorial and brand review. As a brand ambassador, you will need to embrace brand training to become the custodian of our voice and style. You’re not just a writer, you’re a brand advocate., • SEO/GEO mastery. You will dive deep into keyword research and trends to ensure our content is not just read but discovered. You’ll help implement SEO best-practices, leverage firm-approved AI tools to boost our visibility and ranking across search engines., • Stay ahead in the financial landscape. You will keep a finger on the pulse of industry trends and changes. You will balance engaging copy and content with regulatory requirements of our industry. Your insights will help shape our content strategy, AI adoption and keep us ahead of the curve. What you’ll bring: • Digital content expertise. 7+ years of proven experience in creating compelling digital content, preferably in the financial services sector., • SEO, GEO and AI savvy. A solid understanding of SEO principles and experience optimizing content for search. Demonstrated experience with AI-powered content workflows, including LLMs, SEO, and optimizing content for discovery in generative AI experiences (GEO)., • Brand enthusiasm. Willingness to undergo brand training and a commitment to upholding brand standards in all communications., • Editorial perfection. Proven experience in copy writing, editing and proofreading. You have a clear understanding of compliance and regulatory standards to ensure content does not pose a risk to firm. You notice the details other may miss., • A curious mind and an agile attitude. You can thrive in a corporate yet entrepreneurial environment—multiple projects on tight deadlines don’t throw you. You know how to hit the ground running., • Financial acumen. A grasp of financial concepts and the ability to communicate them clearly, succinctly and with a certain charm. Why you’ll love it here: • You will make an impact. Your words directly shape how our audience perceives us and interacts with our brand., • Ours is a collaborative, hybrid environment. You’ll be part of a seasoned team that values creativity, collaboration and excellence. We work hard but we have fun doing it., • An opportunity to grow. You’ll be able to constantly learn and evolve in a dynamic industry. Our marketing group is a global center of excellence. If you’re a digital wordsmith with a passion for finance, a knack for SEO and a commitment to maintaining brand integrity, this is your chance to make a significant impact.

Job Title: Senior Technical Writer. Have least 7 years of experience as a software technical writer creating accessible, user-focused, context-sensitive end-user content. As the ideal new Senior Writer for the User Assistance team, you:.

Content Writer/Blogger/Newsletter Writer - Layout.Thank you for your interest in Volunteering with the Humanity Preservation Foundation and/or Recovery Your Way – it is the volunteers of the organization that make it all happen! As we close out one year we are excited for a great 2026!.The Humanit

Junior Writer Job Duties: • Create effective and compelling copy • Write clear, concise and grammatically correct content that appeals to our various target markets in our brand voice • Support the Head of Content Marketing with writing projects • Convert video and podcast content into blog

Monday-Thursday, 8AM - 5PM, Friday, 8AM - 1PM.Fabuwood is seeking a Content Writer to bring the Fabuwood brand to life through clear, engaging, and on-brand copy.This role is responsible for writing content across all marketing touchpoints including email, blogs, social media, and web, making sure e

Excellent writing, editing, and proofreading skills with a sharp eye for detail. This role is responsible for writing content across all marketing touchpoints including email, blogs, social media, and web, making sure every word reflects Fabuwood's voice and supports our marketing goals. Desire to r

Job DescriptionJob Description.Best Version Media, a growing neighborhood magazine company, is looking for someone local to the Marlton area to coordinate content for a new magazine serving unique, upscale neighborhoods.According to hard monthly deadlines, the Content Coordinator is responsible for:

Scientific Writer/Content Specialist.Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies.We advise on learning strategies and create the right experiences, including online study, virt

Job Title: Senior Technical Writer. As the ideal new Senior Writer for the User Assistance team, you:. Have least 7 years of experience as a software technical writer creating accessible, user-focused, context-sensitive end-user content.

Job Description Senior Marketing & Communications Specialist Location: Philadelphia, PA; Mount Laurel, NJ; or Bedminster, NJ Work Arrangement: Hybrid Weber Gallagher, a growing law firm with more than 160 legal professionals across 13 offices, is seeking an experienced, creative and highly motivated Senior Marketing & Communications Specialist to join our Marketing and Business Development team. Reporting directly to the Chief Marketing & Business Development Officer, this is a highly visible role offering the opportunity to help shape and execute the firm's marketing, communications and brand strategy. The Senior Marketing & Communications Specialist will work closely with firm leadership, attorneys, practice groups and business professionals across offices to strengthen Weber Gallagher's market presence, showcase the firm's capabilities and talent, and support continued growth. We are looking for a strong writer, creative thinker and proactive problem-solver who is equally comfortable developing strategy and rolling up their sleeves to execute it. The ideal candidate brings intellectual curiosity, sound judgment, strong attention to detail and a keen eye for compelling content and design. This is an excellent opportunity for an ambitious marketing professional who wants meaningful responsibility, direct exposure to firm leadership and the ability to make a visible impact. The role offers significant potential for growth for someone who brings ideas, takes ownership and continually looks for ways to elevate the firm's marketing efforts. This role will have access to a shared marketing assistant who can help with projects as needed. Key Responsibilities • Develop and execute integrated marketing and communications initiatives aligned with the firm's strategic, brand and business development objectives., • Help shape and manage the firm's digital marketing strategy, including website content, digital campaigns, social media, paid media and emerging marketing channels., • Develop compelling content that strengthens the Weber Gallagher brand and showcases the firm's attorneys, practices, successes, capabilities and industry knowledge., • Manage the firm's website and its content, keeping it accurate, current and consistent with the Weber Gallagher brand., • Help develop and maintain a firm-wide content calendar across web, social media, email and thought-leadership channels., • Plan and host webinars that showcase the firm's practice groups, working with attorneys on topics, speakers and promotion., • Create, edit and coordinate sophisticated marketing materials, including attorney biographies, practice and industry descriptions, presentations, brochures, client-facing collateral and other brand materials., • Draft and edit press releases, internal communications, website content, social media posts, announcements and other firm communications, ensuring messages are polished, concise and consistent with the firm's voice and brand., • Identify and develop opportunities to increase attorney and firm visibility through thought leadership, speaking engagements, authorship opportunities, media exposure, awards, rankings and professional recognition., • Develop and maintain relationships with relevant media contacts and identify opportunities to position the firm's attorneys as knowledgeable resources on legal and industry developments., • Support the development, planning, promotion and execution of client-facing programs, conferences, sponsorships and firm events., • Develop and manage the strategy, budget, execution and performance of Google Ads and other digital marketing campaigns supporting the firm's consumer-facing practices., • Monitor and evaluate SEO, website performance, social engagement, paid media and other digital analytics and use insights to recommend opportunities for improvement., • Collaborate closely with other members of the Marketing and Business Development team on firmwide priorities, strategic initiatives and special projects., • Help identify and evaluate new marketing technologies, tools and approaches, including opportunities to leverage AI and automation to improve marketing effectiveness and efficiency. Qualifications & Experience • Bachelor's degree in marketing, communications, journalism, public relations, business or a related discipline. Equivalent combinations of education and relevant professional experience will also be considered., • Four or more years of progressively responsible experience in marketing, communications, business development or a related field., • Experience in a law firm or other professional services environment is strongly preferred., • Exceptional writing, editing and proofreading skills, with the ability to translate complex subjects into clear, sophisticated and engaging communications for different audiences., • Demonstrated experience developing professional marketing materials, digital content, presentations, award submissions or comparable collateral., • Strong digital marketing capabilities, including experience with social media, websites, content marketing and digital campaigns., • Experience with Google Ads, SEO, web analytics, email marketing or other digital marketing platforms is highly desirable., • Experience with CRM, content-management, email-marketing or marketing automation platforms is a plus., • A strong visual sensibility and understanding of effective design, layout and brand presentation. Hands-on graphic design experience is a plus., • Strong proficiency with Microsoft PowerPoint and Excel, with the ability to develop polished, professional presentations and marketing materials., • Excellent project-management and organizational skills, including the ability to manage multiple projects, stakeholders and deadlines simultaneously., • Excellent interpersonal skills and the confidence and professionalism to work effectively with attorneys, senior leadership, business professionals, clients, vendors and outside partners., • A high degree of initiative and accountability, with the ability to work independently, anticipate needs and move projects forward without requiring significant oversight. Location & Work Arrangement This is a hybrid position and may be based in Weber Gallagher's Philadelphia, Pennsylvania; Mount Laurel, New Jersey; or Bedminster, New Jersey office.