• Utilize knowledge of construction products, materials, and methods to write specifications for a variety of complex projects and building types. • Support the project team under the guidance of senior staff and the Architect of Record. • Assist in producing Project Manuals utilizing the CannonDesign Master with specification editing software. • Support other specification writers in developing Division 00-14 Architectural sections and custom sections inclusion in the Project Manual. • Support multiple projects and deadlines, contributing to milestone deliverables for various project delivery types. • Collaborate with the Specification Coordinator to support coordination of the Project Manual for all disciplines. • Review and provide revisions to project specific keynotes. • Support review of in-progress drawings to ensure technical specifications are complete and coordinated. • Contribute to the development and improvement of master specifications based on project work and feedback. • Maintain awareness of industry reference standards and resources. Attend industry events as appropriate. • Participate in progress meetings for assigned projects. • Assist project team during CA Phase with shop drawing and product substitution reviews as needed. • Engage with peers through firm-wide specifications writers' meetings to share knowledge and learn best practices. • Support relationship-building with vendors in accordance with the firm's compliance policies. • Support Sustainability goals of the firm. • Seek mentorship from senior staff and contribute to team learning. • Perform work under moderate supervision with opportunities to grow in independence. • May perform other duties as required.

• Developing outlines according to academic/scientific criteria • Direct communication with the client • Producing academic texts using common citation styles (APA, Harvard, German citation style)

• Independently author and review complex clinical and regulatory documents, including clinical trial protocols, clinical overviews, and summaries in CTD/eCTD format for regulatory submissions. • Draft and edit more strategic documents, such as Health Authority briefing books, responses, and publications (abstracts, posters, slide presentations, and manuscripts for scientific journals). • Represent medical writing on internal teams such as the Clinical Trial Team, protocol review committee, and regulatory submission teams. • Lead submission team activities and oversee the preparation of critical documents. • Facilitate team participation in document preparation, including scheduling meetings, developing timelines, and managing document reviews and decisions. • Act as a mentor for new employees and consultants and serve as a role model for junior writers. • Lead the development and review of standard processes and templates. • Support ongoing improvements in cross-functional and global collaboration, sharing best practices and knowledge.

• Create, edit, and refine high-quality content for websites, blogs, newsletters, and digital campaigns. • Collaborate with communications and marketing teams to develop cohesive digital messaging strategies. • Ensure all content aligns with brand voice, style guidelines, and accessibility standards. • Monitor and analyze content performance, using insights to optimize engagement and reach. • Stay ahead of digital trends and best practices to continually enhance content quality.