About Vercel:Vercel gives developers the tools and cloud infrastructure to build, scale, and secure a faster, more personalized web. As the team behind v0, Next.js, and AI SDK, Vercel helps customers like Ramp, Supreme, PayPal, and Under Armour build for the AI-native web. Our mission is to enable the world to ship the best products. That starts with creating a place where everyone can do their best work. Whether you're building on our platform, supporting our customers, or shaping our story: You can just ship things. About the Role:This role has two jobs and you’ll own both. 1) Ship great content. High-quality technical narratives are the baseline. You’ll create work that stands up to scrutiny from senior engineers and executives (including the CTO) as well as seasoned professional writers. The expectation is clarity, accuracy, and grounding in real implementation details, wrapped in tight storytelling. 2) Build the system, agents, and tools that make great content repeatable. We are building the content engine that will define how content is generated in the age of AI. Come build the agents, tooling, workflows, and structure that help our small team ship faster without sacrificing technical credibility or authentic human writing. We’ve got the tokens, and you can help us burn ‘em. You will join a small, high-agency team at the intersection of product, engineering, and go-to-market. We publish for a world where people and AI agents discover, evaluate, and cite information differently than they did in the SEO era. How we workWe treat content like an engineering discipline: quality bars, reusable components, and systems that let us iterate quickly. Just like software engineering, the best people have mastered the craft and can do it by hand, but use AI to dramatically increase their throughput. You’ll work in a stack that may include: - Claude Code (and other code-first LLM tools) for technical exploration, refactors, example generation, and literally building the agents to coordinate our processes. - Shared skills / reusable prompt libraries for consistent drafting patterns and review checklists - Context window management: curating inputs, trimming noise, and keeping high-signal working sets - Memory + retrieval workflows: building a knowledge layer so we don’t rewrite the same background every time - Structured outlines and schemas to make content easier for both humans and agents to navigate and cite If you’ve built systems like this before or you’re excited to, you’ll have a lot of room to shape the approach. When applying, please submit one content sample (blog post or other long-form content) that you feel expresses your ability to excel at this role. If you do not, your application will not be considered. If you’re based within a pre-determined commuting distance of one of our offices (SF, NY, London, or Berlin), the role includes in-office anchor days on Monday, Tuesday, and Friday. If you're located beyond that distance, the role is fully remote. For location-specific details, please connect with our recruiting team. What You Will Do: - Ship excellent content. You’ll write and publish narratives that explain Vercel’s AI Cloud, platform capabilities, and the developer workflows they enable. - Build the content engine that helps the team move faster and stay sharper: - Create repeatable, tech-enabled pipelines for drafting, technical review, publishing, and updates. - Build agents and workflows that support the content development process. - Act as customer zero to pressure test features, SDKs, docs, examples, and messaging for accuracy, clarity, and usefulness. Your content will read like you’ve actually implemented the systems, because you have. - Stay up to date on our products, industry trends, and user needs to ensure the content is relevant and effective. - Review and refine content and code examples for clarity and accuracy. - Keep a tight feedback loop: track performance, learn what people (and models) pick up, and iterate. About You: - You have 5+ years of experience as a Technical Writer, Developer Experience/Advocate Engineer, or in a related role, with a proven track record of high-impact long-form technical writing. - You have hands-on web development experience, and you can reason about real-world tradeoffs. - You know modern frontend tools such as TypeScript, Next.js, and Vercel. - You can collaborate deeply with engineers, ask sharp questions, and earn trust through technical accuracy. - You learn quickly and can turn new domains into clear, comprehensive explanations. - You thrive in a fast-paced environment with high agency and strong ownership. Benefits: - Competitive compensation package, including equity. - Inclusive Healthcare Package. - Learn and Grow - we provide mentorship and send you to events that help you build your network and skills. - Flexible Time Off. - We will provide you the gear you need to do your role, and a WFH budget for you to outfit your space as needed. The San Francisco, CA base pay range for this role is $168,000 - $231,000. Actual salary will be based on job-related skills, experience, and location. Compensation outside of San Francisco may be adjusted based on employee location. The total compensation package may include benefits, equity-based compensation, and eligibility for a company bonus or variable pay program depending on the role. Your recruiter can share more details during the hiring process. Vercel is committed to fostering and empowering an inclusive community within our organization. We do not discriminate on the basis of race, religion, color, gender expression or identity, sexual orientation, national origin, citizenship, age, marital status, veteran status, disability status, or any other characteristic protected by law. Vercel encourages everyone to apply for our available positions, even if they don't necessarily check every box on the job description.

Role Description We are currently seeking a dedicated Clinical Specialist (Radiation Therapist) to join our Global Standards and Content team. In this role, you will play a key part in educating and supporting new users on our proprietary healthcare oncology software and hardware system products. Working closely with product managers, sales, and marketing teams, you will contribute to developing and delivering training strategies for Siemens Healthineers products. Training and Support: - Strategize, coordinate, and facilitate innovative training solutions for hardware products: TrueBeam, IDENTIFY, and Halcyon. - Act as the primary interface between GCS (clinical), Product Marketing and Product Management, ensuring seamless global communication and data dissemination to internal and external customers. Collaboration with Cross-functional Teams: - Collaborate with Product Managers, Product Engineers, Product Marketing, Curriculum Developers, Information Technologists, Internal/External Trainers, and Instructional Designers to develop comprehensive training strategies and materials (documents and/or videos) for internal and external customers worldwide. Training Coordination: - Coordinate and lead customer and employee training classes, with a focus on innovative training solutions. - Provide demo support at local, regional, national, and global customer trade events. - Conduct large group presentations at seminars, training programs, and trade shows. Content Development and Support: - Prepare comprehensive lesson plans based on engineering documentation, field service requirements, and software documentation to address specific implementation questions. - Formulate complementary support training information, including quick tips, procedures/course manuals, and onsite training documentation. - Utilize video creation tools, with proficiency in Camtasia. - Support team members in the implementation of innovative technologies and training solutions. Qualifications - Experience in radiation therapy or related field. - Strong communication and presentation skills. - Ability to work collaboratively in a cross-functional team environment. - Proficiency in video creation tools. Requirements - Must be able to work with controlled technology in accordance with US export control law. Benefits - Medical insurance - Dental insurance - Vision insurance - 401(k) retirement plan - Life insurance - Long-term and short-term disability insurance - Paid parking/public transportation - Paid time off - Paid sick and safe time

Role Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. While this is a remote role, candidates located in the U.S. Eastern Time Zone are preferred to support alignment with clients and business operations. How will you make an impact? - Communication Strategy: Develops and executes a strong communications and content strategy, positioning Thermo Fisher as a top CDMO in the industry. - Market & Competitive Intelligence: Leads market insights and brings perspective to competitive intelligence, while exercising oversight of the Market Intelligence team and their work with key stakeholders. - Content Leadership: Shapes Thermo Fisher’s CDMO thought leadership and voice; develops high-value content marketing strategies that demonstrate our technical acumen, expertise and SME’s. - Leadership: Provides leadership and guidance to their team and ensures high performance. - Strong Collaboration: Team-first mindset when partnering within the Marketing Team, with key stakeholders (leadership, PR team, SME’s, divisions, etc), and externally with agencies, media and vendors. - Media Strategy: Leverage deep understanding of CDMO trade media to create opportunities for Thermo Fisher thought leadership and positioning in the market. How will you get there? - Education: Bachelor’s degree in business, communications or marketing strongly preferred. - Experience: 10-15 years of communications/content experience, required; CDMO experience, required; Strong team player; Strong writing skills. Qualifications - Industry Expertise: Deep experience in the CDMO industry and of the overall drug development process, from early phase through commercialization. - Content Strategy: Expert at creating and shaping content to drive a leadership position in top CDMO journals and publications through paid and earned media. - Content & Communications: Ability to translate complex technical information into compelling messages and relevant content for biotech and biopharma content. - Strategic Thinking: Strong understanding of the CDMO market and business acumen regarding marketing’s role to position and differentiate Thermo Fisher in the market. - Leadership & Influence: Experience leading teams or driving initiatives cross-functionally and without direct authority. - Agency Acumen: Ability to thrive in a fast-paced environment, making quick decisions, and driving teams to deliver high quality work in compressed timelines. Benefits - The salary range estimated for this position based in New Jersey is $170,000.00–$220,000.00. - This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. - We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: - A choice of national medical and dental plans, and a national vision plan, including health incentive programs. - Employee assistance and family support programs, including commuter benefits and tuition reimbursement. - At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. - Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan. - Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount.

Role Description - Support Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) by completing delegated study work. - Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonization Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs. - Collaborate with Site Management & Monitoring, extended study team and external vendors in collection of regulatory and other essential documents. - Coordinate regular Quality Checks (QC) and review of the TMF, ensuring continual inspection. - Contribute to electronic applications/submissions by creating and managing clinical-regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory. - Proactively plan and collate the administrative appendices for the CSR. - Initiate and maintain production of study documents, ensuring template and version compliance per study specific requirements. - Set-up, populate and accurately maintain information in tracking and communication tools and support team members in the usage of these tools. - Support the set-up, maintenance and close-out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant stakeholders to fulfil AstraZeneca compliance and meet the regulatory authority needs. - Support the GSD/GSAD with tracking, reconciliation and follow-up of the study budget/payments in relevant systems. - Contribute to application, coordination, supply and tracking of study materials and contribute to collection of study supplies, if required, at the study close-out. - Coordinate administrative tasks and logistic support throughout the conduct of the study, audits and regulatory inspections, according to company policies and SOPs. - Lead the practical arrangements coordination and contribute to the preparation of internal and external meetings (e.g., study team meetings, committee meetings, monitor meetings, Investigator meetings and virtual meetings). Liaise with internal and external participants and/or vendors. Qualifications - Education in medical or biological sciences or discipline associated with clinical research preferred. - Proven organizational and analytical skills. - Previous administrative training/experience. - Computer proficiency in day-to-day tasks. - Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines. - Excellent verbal and written communication in English. - Demonstrate ability to work independently, as well as in a team environment. - Willingness and ability to train others on study administration procedures. - Global study support experience preferred but not required. - Experience managing eTMF and CTMS systems is required (Veeva Vault experience preferred). Benefits - Various annual leave entitlements. - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance. - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.