Role Description Think Academy specializes in providing online math education for students in North America. Our curriculum aligns with U.S. Common Core State Standards (CCSS) and supports students across upper elementary, middle school, and high school levels. We are currently seeking Remote Math Tutors to support project testing and ongoing curriculum development. - Deliver one-on-one online math lessons for students in Grades 5-8 across North America, aligned with the CCSS framework. - Teach in English using interactive and student-centered methods to promote engagement, strengthen core concept understanding, and address questions in real time. - Prepare lesson content based on individual student needs, ensuring well-structured and high-quality instruction. - Provide timely feedback and targeted guidance to support student understanding and continuous improvement. Qualifications - Bachelor’s degree or above; majors in Math, Education, or related fields are preferred. - Teaching experience or a valid teaching certificate is highly preferred. - Available and willing to work during weekday evenings and weekends. - Excellent communication and interpersonal skills. - Bilingual in Mandarin Chinese is preferred. Requirements - Pay starts from $20–25/hr, with opportunities for promotion and salary increases twice a year. Benefits - Think Academy is an equal opportunity employer. - All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status. - Will not be discriminated against on the basis of disability.

Role Description The Director Medical Writing is an expert medical writer, responsible for writing and coordinating the writing of various clinical and regulatory documents including: - Protocols/amendments - Investigator brochures - Clinical study reports - NDA/BLA submission documents The Director Medical Writing will work closely with cross-functional teams to manage the preparation of written clinical and regulatory documents, ensuring that they are of high quality and completed in a timely fashion compliant with SOPs, ICH/GCP/regulatory guidelines, and company goals. The Director will also manage and mentor more junior writers and will be seen as a key SME for medical writing providing leadership across global teams. Work Model: Remote - Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed. Responsibilities - Development and implementation of document strategy for clinical and regulatory documents including writing, editing and/or reviewing of protocols, investigator brochures, clinical study reports, INDs, eCTD/NDA clinical summaries, and briefing books. - Develop and maintain a strong network of internal relationships to actively support cross-functional project team(s) representing Clinical Regulatory Writing. - Provides strategic insight for timely and accurate deliverables, negotiating timelines as necessary. - Drives and executes writing strategies across clinical development program(s) ensuring effective collaborations with other functional areas. - Review, edit, and ensure quality of documents or sections of documents prepared by functional area representatives and/or contract writers as required and ensure adherence to standards. - Effectively manages vendor/contract writers and forecasts external resources as needed to support internal deliverables. - Proactively implements clinical transparency and disclosure practices in document development (e.g. Policy 70, Clintrials.gov, etc.). - Provides coaching, training, and supervision of medical writing staff as applicable. - Provides department leadership by proposing and overseeing new initiatives and capabilities. - Work across departments to help set priorities and establish best practices for document preparation and review. - Manages resource planning including program and team forecasting. Qualifications - BS, MS, or doctorate in a scientific or medical field with 10 years working as a medical writer in the biotechnology/pharmaceutical industry (advanced degree preferred). - Demonstrated experience in medical writing, editing, and clinical development; has written protocols, IBs, CSRs; worked on at least one eCTD/NDA submission. - Deep understanding of the key requirements for regulatory submissions as stipulated in FDA and ICH guidelines for preparation of INDs, NDAs/BLAs and MAAs. - Strong leadership, planning, and project management skills, along with initiative and ability to be productive with minimal supervision and minimal administrative support. - Proven ability to develop and implement medical writing processes and standards. - Exceptional oral and written communication skills. - Understands and effectively responds to multicultural communication styles and business practices with alliance partners and internal colleagues. - Flexible; adapts work style to meet organization needs. - Strong organizational abilities and experience in a multitasking environment. - Motivated, self-directed, and able to work autonomously and in team settings to meet aggressive organizational goals. - Dedication to quality and reliability. - Excellent computer skills (Microsoft Office Suite, Power Point, Adobe Illustrator, figures and graphic design; Project and Visio a plus). - Ability to build and maintain effective partnerships, both internally and externally, and experience working successfully on matrixed teams. - Holds self and others accountable for adherence to high ethical standards; adopts and maintains the utmost integrity and respect for colleagues at all levels. - Rare disease experience and a strong understanding of metabolic genetics or metabolic bone disease a plus. Requirements - The typical annual salary range for this full-time position is $207,600 — $256,400 USD. - This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment. Benefits - Generous vacation time and public holidays observed by the company. - Volunteer days. - Long term incentive and Employee stock purchase plans or equivalent offerings. - Employee wellbeing benefits. - Fitness reimbursement. - Tuition sponsoring. - Professional development plans. - Benefits vary by region and country.

Role Description You'll write the in-product copy that shapes how users experience the app — button labels, onboarding flows, error messages, tooltips, and push notifications. You'll work embedded in the product design team, contributing to features from early concept through to shipped. - Write clear, concise copy for UI components, flows, and empty states - Collaborate with product designers and PMs from brief to launch - Conduct content audits and rewrite copy that isn't working - Maintain and evolve the product voice and tone guidelines - Review designs for copy consistency and UX writing best practices Qualifications - Strong written English with a natural, human voice - Understanding of UX principles — you think in user flows, not just words - Confident working in Figma or similar design tools - Collaborative — you work well with designers, PMs, and engineers Requirements - Portfolio of UX writing work from apps or web products (nice to have) - Experience with content strategy or information architecture (nice to have) - Background in copywriting, journalism, or a related writing discipline (nice to have) Benefits - $700–$1,100 USD/month based on experience - Fully remote with flexible hours - Embedded in product design — high visibility and impact - Paid leave - Path to Content Design Lead or Product Strategy roles

• Provide consultation services to students in the dissertation process, as well as doctoral and master’s-level assignments. • Provide overflow support to the Writing Center as needed, providing personalized guidance to students on a wide range of assignments including, but not limited to, essays, research papers, and dissertations. • Ensure feedback is delivered promptly, meeting established deadlines and service standards. • Maintain regular communication with the Writing Center leadership to align with best practices and improve student outcomes. • Facilitate workshops and writing boot camps, including curation and delivery of related materials, virtually as needed. • Create and curate content for dissertation support resources, such as handouts, explanations, and tutorials. • Provide copyediting services for the University’s research journal prior to publication. • Attend Writing Center team meetings and participate in professional development activities. • Effectively use relevant software and platforms, including Learning Management Systems (Moodle), video conferencing tools (Zoom), and document editing tools (Microsoft Word, Google Workspace). • Adapt teaching methods to support second-language learners and students from diverse linguistic and cultural backgrounds. • Assist in Writing Center projects, such as piloting new programs or developing advanced resources. • Track and report student progress and engagement to Writing Center leadership. • Apply knowledge from certifications (e.g., TESOL or advanced academic editing) as applicable.