• Write hooks, scripts, and threads that make products impossible to ignore at launch • Own copy for X and LinkedIn — each platform's grammar, written fluently • Iterate in real time based on what the data says, not gut feeling

Role Description Our content writers drive 100 million views every month on X and LinkedIn. You'll be writing for the biggest accounts in tech — the founders who will be this generation's Steve Jobs, backed by Sequoia, Khosla, and A16Z. You'll be working directly with them. Qualifications - High IQ — neurodivergent is a plus - Terminally on X. 20+ hours a week minimum. - Know who Clav is - You’ve read Breakthrough Advertising - You have a swipe file with hundreds of entries - Meme culture is research, not entertainment - You think "good enough" is a form of failure - Top 1% problem solver - Workout regularly Requirements - You have posts that crossed 1M+ impressions and can explain exactly why each one worked - You write fast without sacrificing quality - You think about writing the way engineers think about systems: testable, iterable, improvable - You know the difference between a post that gets shares and one that gets just impressions — and which one you need when - You've written for a founder or executive and made their voice feel authentic - 5+ pieces at 1M+ impressions? Consider yourself hired. (Close but not there? We'll train the rest.) Benefits - Emmy winners, ex-Mr. Beast filmmakers, elite creative strategists with 3B+ organic views combined - Every week we engineer viral launches for the companies defining the next decade of tech — hundreds of millions of views, zero paid distribution

• Prepares and reviews clinical/regulatory documents to support all phases of drug development • Leading the writing activities for all regulatory documents for a project team • Identifying and managing contractors • Planning activities for New Drug Applications (NDAs) and global Marketing Authorization Applications (MAAs) • Building and managing the submission writing team • Authors and manages the authoring process for all clinical/regulatory documents • Leads and provides subject matter expertise to the core authoring team • Ensures document content is clear, concise, strategic, and well positioned for public disclosure • Supports authoring best practices and provides continued training to teams • Represents Medical Writing Department on project teams • Mentor and may manage internal staff

• Provide technical writing, editing, and document management support to a federal law enforcement organization responsible for border security technology and operations. • Communicate complex information clearly and concisely to diverse audiences through written materials. • Review, edit, and refine documents to ensure accuracy, clarity, and consistency. • Develop content for reports, briefings, and presentations tailored to stakeholder needs. • Adhere to agency style guides and formatting requirements for official communications. • Edit station profile updates and requirements documents for leadership review. • Refine operational requirements documents for USBP and CBP leadership, ensuring compliance with agency standards. • Support efficient routing and approval processes for senior leadership. • Analyze and edit executive-level documentation, briefings, internal correspondence, and publications, marking substantive changes as needed. • Determine and apply appropriate levels of review (proofreading, copyediting, substantive editing). • Develop executive summaries and briefings from larger documents. • Collaborate with authors and subject matter experts to clarify message, audience, style, and publication schedule. • Ensure grammar, structure, flow, readability, and presentation meet client and industry standards. • Oversee publication workflow throughout the approval process, serving as the final reviewer when necessary. • Manage documentation, project, and task workflows. • Assist with publication maintenance, future activities, and integration with broader agency initiatives to support program growth.