Role Description The American Association for the Advancement of Science (AAAS) and Science magazine have an exciting opportunity for a full-time Senior Editor for the Commentary section. The editor will handle primarily Perspectives in biology. A broad knowledge of neuroscience is desirable but familiarity across the biological sciences is necessary. Perspectives provide accessible, broadly interesting, and authoritative analyses on the most important recent scientific developments. They can be paired with papers in the journal but also be “stand alone” pieces on emerging topics. The position also covers opinion pieces, including Expert Voices columns. The editor works with the Visuals and Media teams to create striking explanatory graphics and multimedia, while ensuring excellent customer service to our authors. What You’ll Do: - Invite, edit, and publish Perspectives every week in Science - Handle the peer-review of “stand alone” Perspectives - Handle Expert Voices columns and possibly other opinion pieces - Work with social and multimedia teams for communicating scientific concepts - Network with the scientific community through meetings and professional contacts and identify topics and authors for Perspectives - Contribute to other parts of the magazine including special issues and “In Other Journals” Qualifications - A PhD and postdoctoral research experience in a relevant field - At least five years of experience as a commissioning editor with proven ability to meet deadlines, commission commentary, and edit text to achieve accessibility to a broad audience - Familiarity and ease with publishing and editing software (MS Office, Adobe Professional) - Comprehensive knowledge of scientific research methods to discuss technical issues with authors - Excellent outreach skills to identify and select the best authors for the journal - Exceptional written, communication, and listening skills to communicate with authors and members of the editorial and production teams - Time management: A proven ability to work efficiently to meet competing deadlines - Exceptional editing skills to ensure efficient and high-quality standards of writing - Knowledge of best practices in commissioning and peer review to ensure fairness, diversity, and ethical handling of manuscripts - Ability to make informed, fair, and consistent decisions about submitted content Requirements - Location: Offices in Washington, DC and Cambridge, UK. Remote work is possible. - If you are not located in or able to work from a location where AAAS has a business presence, you may not be eligible for this position. - Contact our Talent Team at jobs@aaas.org with any questions regarding your eligibility. Benefits - Paid vacation leave - Paid sick leave - Paid holidays - Health insurance - Flexible spending account - Dental insurance - Life insurance - Vision insurance - Retirement benefits - Short- and long-term disability - Each subject to the terms of the applicable program Application Process Submit a resume and cover letter outlining qualifications and interest in the position by July 3, 2026. Applications are reviewed on a rolling basis. A Recruiter will contact you with next steps if you are selected for an interview. The anticipated initial rate of compensation for this position is $95,000 – $100,000 per year (for candidates hired in the US). Any actual offer of employment, reflecting the total compensation package and benefits, will be made in the sole discretion of AAAS and will be based on a variety of factors, including years of experience, depth of experience, and other relevant factors. AAAS reserves the right to amend or modify its employment benefits and compensation structure at any time. AAAS is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender, gender identity, national origin, age, disability, veteran status, or other protected category. AAAS uses E-Verify to confirm the employment eligibility of all newly hired employees. No visa sponsorship is available for this position.

• Own the end-to-end proposal process for grant applications, funding proposals, government submissions, partnership applications and other supporting documentation. • Research relevant grant and funding programs, monitor new funding opportunities aligned with company priorities, and support evaluation of eligibility and fit. • Partner with internal team members to gather technical, operational, and financial information, translate complex ideas into clear, compelling narratives and coordinate inputs across teams to meet deadlines. • Research, write, and edit all proposal sections. • Maintain proposal templates and reusable content, organize supporting materials, metrics, and company information, and help standardize proposal processes as we grow. • Track grant and proposal timelines, manage submission calendars and requirements and ensure applications are complete, accurate, and submitted on time.

Role Description An SEO, web design and development, and product-positioning agency serving startups, tech companies, and B2B brands is looking for an SEO Copy Editor to strengthen the craft side of its content programs and own editorial quality across multiple client brands. The team is small, fast-moving, and works directly with founders, marketers, and engineers building real products. Content runs through structured, repeatable systems — from keyword research to brief, draft, and publish — and the editorial bar is high: original, accurate, genuinely useful work that stands out in a crowded space. Day-to-day, this role oversees a team of SEO writers, refines tone and accuracy, and edits both human and AI-generated drafts for clarity and consistency. It maintains brand voice guidelines per client and aligns writing with keyword strategy, topical depth, and internal-linking goals. Success means every published piece meets editorial and technical SEO standards, on deadline, across several content calendars at once. Qualifications - 4+ years of writing or editing experience for B2B, SaaS, or marketing-focused companies - Hands-on experience with SEO tools including Ahrefs, SEMrush, and SurferSEO - Working knowledge of SEO fundamentals — search intent, content structure, and on-page optimization - Demonstrated experience editing other writers' and AI-generated drafts for clarity, accuracy, and consistency - Experience building and maintaining brand voice guidelines across multiple clients or brands - C1+ English (CEFR) for editorial-quality writing and editing Requirements - Experience building editorial QC checklists and templates across multiple content calendars - Background in an SEO or content agency managing several client brands simultaneously - Conversion-focused copywriting experience (landing pages, lead magnets, product explainers) - Experience aligning content with internal-linking and topical-cluster strategy Benefits - Competitive Salary: Based on experience and skills - Remote Work: Fully remote—work from anywhere - Team Incentives: Recognition for maintaining 100% CRM hygiene and on-time reporting - Generous PTO: In accordance with company policy - Health Coverage for PH-based talents: HMO coverage after 3 months for full-time employees - Direct Mentorship: Guidance from international industry experts - Learning & Development: Ongoing access to resources for professional growth - Global Networking: Connect with professionals worldwide

Role Description The MWS Consultant I plays a critical role in authoring and managing regulatory documents, supporting client regulatory strategies, and ensuring high-quality deliverables that align with client expectations and regulatory standards. This role is responsible for leading document development efforts, coordinating regulatory projects, and collaborating with cross-functional teams to meet diverse client needs across varying stages of development. The MWS Consultant serves as both a technical contributor and project owner, ensuring document accuracy, submission readiness, and adherence to regulatory requirements while maintaining strong client relationships and delivery excellence. The MWS Consultant I position is eligible for remote work based on company requirements, with no minimum in-office requirement. Key Responsibilities - Author a variety of regulatory documents, including Clinical Study Reports (CSRs), study protocols, and client submission materials. - Lead the development of complex modules (e.g., Module 2 summaries, Briefing Documents, Orphan Drug, Fast-Track, and Breakthrough Designation applications). - Apply quality control and submission-readiness processes to deliver high-quality documents within agreed client timelines. - Serve as a project owner by tracking timelines, adjusting schedules, and coordinating with clients to address evolving demands. - Plan for and anticipate project challenges, update visual timelines, and maintain adherence to deadlines. - Facilitate client interactions, including meetings, inquiries, and feedback discussions, while building and maintaining client trust. - Ensure consistency, accuracy, and alignment across documents with client updates and applicable regulatory standards. - Collaborate with cross-functional teams to ensure the quality and accuracy of regulatory documents. - Contribute to the development of regulatory strategies for early-stage and smaller clients. - Provide guidance on tools, document management systems, and client SOPs. - Engage in continuous learning through exposure to new document types, processes, and industry best practices under senior mentorship. Qualifications - An advanced degree (e.g., M.S., PharmD, Ph.D., or M.D.) in life or health science is preferred. - RAC certification is beneficial. Requirements - 3+ years industry experience. - Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), Teams, and MS Project. - Familiarity with regulatory document management systems, such as Veeva Vault. - Experience with regulatory submissions and understanding of global regulatory standards. - Strong foundation in medical writing, regulatory writing, and interpretation of scientific content. - Knowledge of pharmaceutical and biopharmaceutical environments, including clinical trials and regulatory submissions. - Effective written and verbal communication skills, with the ability to communicate complex scientific and regulatory information clearly and concisely. - Exceptional project and time management skills, with the ability to prioritize multiple projects and adjust timelines proactively. - Patient and empathetic approach, especially in cross-cultural and client-facing environments. - Positive attitude toward feedback and a willingness to apply it for continuous improvement. - Strong critical thinking and data analysis skills to ensure scientific claims align with evidence and regulatory requirements. - High attention to detail, ensuring alignment and accuracy across multiple document reviews. Benefits - Market competitive base salary and annual incentive plan. - Robust benefit offerings. - Ongoing recognition and career development opportunities. - Generous flexible paid time off program. - Company paid holidays. - Flexible working hours. - Fully remote or hybrid work options for some roles. - Office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.