• Review, analyze and code diagnostic information in patient charts; identify coding opportunities for improved coding accuracy • Validate missed coding opportunities • Ensure compliance with established coding guidelines, third party reimbursement policies, regulations and accreditation guidelines • Audit patient charts to ensure accurate coding

• Mentors and leads less experienced medical writers on complex projects, as necessary. • Acts as lead for assigned med info writing projects. • Manages and coordinates medical information activities within and across departments with minimal supervision. • Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers). • Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide. • Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions. • Experience in developing or supporting a variety of documents that include, but not limited to: Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations. • Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate. • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables. • Serves as peer reviewer on internal review team providing review comments on draft and final documents. • Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.

• Review patient medical records (charts) for completeness, accuracy, and compliance with ICD-10-CM coding guidelines and CMS risk adjustment criteria. • Identify documentation gaps or opportunities that impact HCC capture and risk scores. • Utilize AI-enabled CDI platforms, electronic health records (EHR), and data dashboards to analyze trends, prioritize chart reviews, and flag discrepancies. • Work closely with primary care providers, specialists, and other clinical staff to clarify documentation and educate on best practices, when required. • Collaborate with coding, billing, compliance, and analytics teams to align goals and implement CDI strategies, when required. • Support the execution of cross-functional projects aimed at improving data integrity, documentation quality, and risk adjustment outcomes. • Maintain accurate tracking and reporting of CDI queries, provider responses, and documentation improvements in designated systems or databases. • Stay up to date on current CMS guidelines, ICD-10-CM updates, HCC risk adjustment models (CMS-HCC, RxHCC), and relevant healthcare regulations.

• Mentors and leads less experienced medical writers on complex projects, as necessary. • Acts as lead for assigned writing projects. • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. • Develops or supports a variety of documents that include, but not limited to: Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations. • Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate. • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables. • Serves as peer reviewer on internal review team providing review comments on draft and final documents. • Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget. • Performs on-line clinical literature searches, as applicable. • Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics. • Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats) • Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets. • Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing. • Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership. • Completes required administrated tasks within the specified timeframes. • Performs other work-related duties as assigned. • Minimal travel may be required (less than 25%).