Senior Editor, Newsletters Editorial Remote - Eastern US The Opportunity Everyday Health is looking for a Senior Editor to create content to deepen our relationships with our readers and grow traffic outside of organic search. The editor will work closely with our Audience Development and Commerce teams and be responsible for executing a newsletter strategy that inspires, educates, and converts through compelling storytelling and insights. The editor will also have proven experience crafting narratives that drive engagement and revenue while maintaining a consistent, on-brand content voice. The applicant must be a highly creative, independent editor with the ability to prioritize and excel in a fast-paced environment. The applicant must have strong communication and project management skills and should be comfortable working cross-functionally to meet project deadlines. Key Responsibilities: - Execute on a strategy to test and evolve 3-5 newsletters to be content- and commerce-forward, including helping to develop the content and writing it - Develop content to support monetization opportunities within newsletter products - Contribute to a podcast content strategy, including writing a newsletter to support the podcast - Look for ways to repurpose social video and other content Job Qualifications - 7+ years of digital writing and editing, including experience with an online Health, Wellness, News and/or Lifestyle brand - Demonstrated experience writing newsletter content - Demonstrated experience working on multi-platform content and initiatives - Ability to meet deadlines - An understanding of performance and audience data and using it to inform content strategy - The ability to distill nuanced health information into easily understandable, accurate, and engaging copy on deadline - Strong editorial judgment - Organized, with good verbal and written communication skills, attention to detail, and the capacity to work effectively and across departments - Experience working in a CMS - Experience with AI - Bachelor’s degree required, preferably in Journalism, Communications, English, Marketing, or related field Life at Everyday Health At Everyday Health Group, the Health & Wellness division of Ziff Davis, we work in a culture of collaboration and welcome those who desire to join our growing global community. We believe in careers versus jobs and people versus employees. We seek enthusiastic individuals with an entrepreneurial spirit looking for an environment that rewards your best work. Everyday Health offers competitive salaries in addition to robust, health and wellness-focused benefits, including comprehensive medical, dental and vision coverage, as well as life and disability benefits. Our employees enjoy Flexible Spending Accounts (FSAs), a 401(k) with company match, and an Employee Stock Purchase Plan. We are committed to work-life balance with Flexible Time Off, Volunteer Time Off and paid holidays. We offer family building and caregiving support and generous Family Care and Parental leave, when you need it. We also provide Fitness Reimbursement and access to wellness programs, ensuring our team stays healthy both physically and mentally. Our Culture and Values We created our values together to guide our collective purpose and pursuits. We are collaborators and problem solvers. We empower one another to make informed decisions and to be enabled towards action. We embrace success. We recognize that innovation can spark and be born from any of us no matter our individual role or background. We encourage open mindedness and sensitivity to each other and our environment. Our personal and professional passions get ignited, nurtured and supported. We value that doing is greater than talking as the most measurable means of impact. Our collective purpose to deliver enlightened audience experiences with trusted brands is what drives the success of our business and our professional satisfaction.

The Batch, Andrew Ng's weekly newsletter on artificial intelligence, seeks freelance writers who have a clear, detailed understanding of machine learning technology! The Batch reaches over 2 million machine learning professionals and students worldwide. You can see our archive here: deeplearning.ai/thebatch We're looking for graduate students and postdocs in machine learning to write summaries of recent research. This is a paid freelance position (fee negotiable). It involves summarizing research papers in our established format and in clear language that's understandable by readers who may be new to the field. Would you like to educate up-and-coming practitioners and possess a combination of machine-learning expertise and English-language writing skill? Please apply.

iT1, a leading national technology solutions provider headquartered in Tempe, Arizona, is seeking a skilled and experienced Document Manager and Proposal Writer to join our growing team. Recognized as one of Arizona’s Best Places to Work for more than a decade, iT1 is committed to excellence, collaboration, and employee growth. In this role, the Document Manager and Proposal Writer will support revenue growth through the creation, management, and execution of high‑quality proposals, contracts, and business documentation. This position plays a critical role in responding to commercial and federal RFPs/RFQs, managing the end‑to‑end contract lifecycle, and ensuring alignment across sales, legal, and operations.

Title: Director/Senior Director, Medical Writing Department: Regulatory Affairs Reports To: VP, Regulatory Affairs Status: FTE About vTv vTv Therapeutics is a clinical stage biopharmaceutical company focused on developing oral, small molecule drug candidates. vTv has a pipeline of clinical drug candidates led by cadisegliatin, a potential adjunctive therapy to insulin for the treatment of type 1 diabetes. vTv and its development partners are pursuing additional indications, including type 2 diabetes and other chronic conditions. Description vTv is seeking a Director/Senior Director, Medical Writing to lead the strategy, development, and delivery of high-quality clinical and regulatory documents supporting our global clinical development programs - including clinical study protocols, investigator brochures, clinical study reports (CSRs), briefing documents, INDs, NDAs/BLAs, MAAs, safety reports, and scientific publications. This role partners closely with Regulatory Affairs, Clinical Development, Biostatistics, Clinical Operations, and other functional teams to ensure the timely preparation of scientifically rigorous and regulatory-compliant documents across the product lifecycle. The Director/Senior Director serves as the medical writing lead for major development programs, ensuring alignment of messaging and scientific integrity across regulatory submissions, clinical documentation, and external communications. This is a unique opportunity to contribute to the development of a potential first-in-class therapy in diabetes, working in a collaborative and science-driven environment. This position is fully remote. Key Responsibilities - Medical Writing - - Provide strategic leadership and oversight of the Medical Writing function, ensuring the delivery of high-quality clinical and regulatory documentation. - Establish document standards, templates, style guides, and best practices aligned with regulatory expectations (ICH, FDA, EMA). - Oversee document planning, timelines, and resource allocation across programs to ensure on-time delivery of key regulatory and clinical deliverables. - Lead identification and management of external medical writing vendors and consultants as needed. - Maintain awareness of evolving regulatory guidance and industry best practices relevant to clinical and regulatory documentation - Supervise (directly or indirectly) a team of medical writers and external writing vendors, and may recruit, manage, mentor, and develop writing staff. - Clinical and Regulatory - Serve as the medical writing lead for assigned development programs, partnering with clinical, regulatory, and statistical leaders providing strategic guidance and development to ensure clear and consistent scientific communications. - Lead the preparation and review of major clinical documents as applicable, including: - Clinical study protocols and protocol amendments - Clinical study reports (CSRs) - Investigator brochures (IBs) - Safety narratives - Scientific manuscripts and conference abstracts - Ensure scientific accuracy, clarity, and consistency across clinical documents. - Collaborate with cross-functional teams to present complex clinical and scientific data into clear, regulatory-compliant documents. - Manage clinical development processes and document archival requirements - Provide strategic input into regulatory submissions, ensuring consistency of messaging across documents and alignment with regulatory strategy. - Support preparation of documents for regulatory meetings with agencies (e.g., FDA Type B meetings, End-of-Phase meetings, advisory committees) and major regulatory documents, including IND, CTA, NDA/BLA, and MAA submission components (e.g., ISS/ISE summaries, Module 2 documents, Clinical overviews, etc.) - Leadership - - Serve as the strategic medical writing representative on program teams and development governance committees. - Provide expert guidance on document strategy, messaging, and expectations. - Contribute to corporate initiatives related to scientific communication, publication strategy, and document quality standards. - Mentor internal staff and foster a culture of scientific rigor, clarity, and excellence in medical writing. - Represent vTv on high impact/priority task forces across vTv or external to the company. EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: - Advanced degree preferred (MS, PhD, PharmD, MD, or equivalent scientific discipline preferred). - 12–15+ years of medical writing experience within the pharmaceutical or biotechnology industry, CRO, or related environment. - Extensive experience preparing clinical and regulatory documents supporting INDs and NDAs/BLAs. - Demonstrated leadership of complex cross-functional writing projects and submission programs. - Experience managing medical writing teams and external vendors preferred. Skills - Exceptional scientific writing and editing ability. - Strong strategic thinking and problem-solving skills. - Ability to translate complex scientific data into clear, concise, and regulatory-compliant documentation. - Strong cross-functional leadership and collaboration skills. - Excellent communication and interpersonal skills with the ability to influence multidisciplinary teams. Knowledge - Expert knowledge of ICH guidelines and global regulatory submission standards. - Familiarity with FDA and EMA expectations for clinical documentation and regulatory submissions. - Experience with word templates, electronic submission formats (eCTD) and document management systems. LICENSES/CERTIFICATIONS: - None required - AMWA certification preferred but not required. TRAVEL REQUIREMENTS: - Ability to travel occasionally for internal meetings, regulatory interactions, or scientific conferences. - Requires approximately 5 - 10% travel. - This is remote position