• 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

• Leads the preparation of complex scheduled and unscheduled aggregate safety reports across multiple product types and regulatory regions. • Develops strategic approaches for challenging safety submissions. • Reviews and approves high-complexity safety documents. • Manages meeting logistics including scheduling, agenda drafting, and minute preparation. • Designs and implements advanced signal detection plans tailored to specific product profiles. • Leads signal detection for priority products by conducting expert-level analyses. • Authors and reviews high-priority signal assessment reports and health authority response documents. • Prepares and handles reviews of health authority response documents. • Collaborates with cross-functional teams to ensure RMPs are scientifically robust and compliant. • Demonstrates deep expertise in safety profiles across a wide range of therapeutic areas.

• Leads or contributes to the preparation and compilation of aggregate safety reports. • Reviews and finalizes safety documents for accuracy and compliance. • Coordinates submissions to regulatory authorities. • Conducts literature searches and systematic reviews. • Identifies complex data discrepancies. • Supports development of Risk Management Plans. • Actively contributes to safety strategy discussions. • Serves as primary client liaison for projects. • Monitors KPIs and SLAs for assigned deliverables. • Mentors junior team members by providing training.

• Independently lead the preparation/update of complex aggregate safety reports across multiple product types • Manage the distribution of final reports to stakeholders, including partners and health authorities • Leads advanced safety signal detection and management for key products • Collaborates with cross-functional teams to analyze complex safety data • Provides strategic scientific expertise across therapeutic areas