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

• Take ideas and topics, research them thoroughly, and turn them into clear, well-structured, useful content. • Write across formats: blog posts, LinkedIn, Substack, and YouTube scripts. • Go deep on technical and finance-adjacent subjects and write about them with credibility. • Help scale our publishing volume while holding a very high bar on quality. • Care whether each piece worked: that it got read, ranked, and shared, and learn from what did and didn't.

• Write and/or review multiple lesson scripts that address specific parts of the NZ Y7-10 Mathematics curriculum • Lessons will cover a depth of knowledge and align with the set curriculum standards