• Ensure scientific information is presented clearly and accurately • Coordinates medical writing activities within and across departments • Leads the resolution of comments from the client • Ensures source documentation is managed appropriately • Provides technical support, training, and consultation to department • Mentors and leads less experienced medical writers on complex projects

• Develop and deliver original, accurate, high-quality content (manuscripts, slides, and other editorial assignments) • Provide high‑quality editorial oversight for both project work and business development efforts • Function as a scientific and therapeutic expert for assigned project teams • Function as the primary writer for assigned accounts

• Perform medical literature research and data analysis • Develop medical and scientific copy • Support project pitch development and delivery • Provide medical and scientific support during client meetings • Edit copy for correctness and stylistic consistency • Prepare and submit content for medical legal regulatory review • Collaborate with Design to ensure visuals are scientifically accurate • Assist with the creation of budget estimates for new/revised projects • Educate team members on scientific constructs

• Develop and maintain a structured research roadmap aligned with organizational clinical priorities • Organize research initiatives across multiple clinical programs and stakeholders • Establish standardized processes for study design, data requests, analysis, and publication timelines • Coordinate cross-functional collaboration with clinical, data, product, and operations teams • Analyze large clinical and administrative datasets (e.g., EHR, monitoring data, claims when available) • Conduct outcomes, quality, and utilization analyses using appropriate statistical methods • Partner with data teams to define data requirements and ensure data quality and integrity • Translate analyses into clinically meaningful insights and conclusions • Lead authorship and coordination of abstracts, posters, and manuscripts for CV conferences and journals • Draft and revise manuscripts in collaboration with clinical leaders and co-authors • Manage submission processes for conferences and peer-reviewed journals • Support responses to reviewer comments and revisions • Support IRB submissions, exemptions, and regulatory documentation as needed • Ensure research activities comply with ethical, regulatory, and data governance standards • Maintain documentation for study protocols and approvals • Serve as a key liaison between clinicians, leadership, and external research collaborators • Support joint research initiatives with partners, payors, and academic institutions • Present findings internally and externally as needed