• 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.

Role Description Teach English to European students online from home in a structured virtual classroom environment. - Conduct live English lessons according to provided guidelines - Log in to the teaching platform before class and manage your schedule - Provide corrections and clear explanations during lessons - Evaluate student performance based on structured criteria - Assign and conduct tests or assessments when required - Deliver personalized feedback tailored to each student’s needs Qualifications - Clear, native-like English accent - Minimum 1 year of teaching experience - Ability to manage students of any age group - Reliable home workstation with stable internet and power supply - Energetic, cheerful, and professional demeanor Requirements - Working Hours (Choose one shift): - Night Shift: Monday – Friday, 9:00 PM – 5:00 AM - Day Shift: Monday – Friday, 8:00 AM – 6:00 PM; Saturday 8:00 AM – 11:00 AM - Evening Shift: Monday – Friday, 6:00 PM – 12:00 AM