• Accurately review, interpret, and abstract clinical patient data from various electronic health record (EHR) systems, paper charts, and other source documents. • Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) to interpret, classify and categorize abstracted clinical data points. • Utilize specialized data management software (e.g., REDCap, registries, and custom built EDC systems) to enter, track, and maintain clinical data integrity. • Aid cross-functional teams in translating clinical and data abstraction and encoding requirements. • Apply and support establishing program specific clinical data management best practices (CGDMP) and good clinical practice (GCP). • Apply industry standard best practices for utilizing real-world data for research, quality monitoring, and regulatory reporting. • Conduct peer reviews on medical record data interpreted and encoded by abstraction peers. • Maintain strict adherence to all project and research protocols, institutional review board (IRB) requirements, HIPAA regulations, and data management best practices. • Participate in the development and refinement of abstraction and quality guidelines, tools, and standard operating procedures. • Provide timely and accurate daily, weekly, or monthly abstraction submissions and productivity reporting.

• Travel ~50% in person customer facing in collaboration with Natera commercial representatives and/or medical affairs colleagues to provide clinical knowledge and support for Prospera • Provide in-depth education and support to transplant coordinators and allied health professionals surrounding the benefits of implementing routine transplant rejection monitoring, specifically using Prospera. • Collaborate with the MSLs and medical directors in providing additional information to healthcare providers as it pertains to Natera products • Engage in continuous learning in organ transplantation to maintain scientific and clinical expertise • Support ongoing clinical trial and research initiatives at academic institutions and/or study sites in collaboration with the MSL team • Performs other duties as assigned

• Analyze complex genomic datasets leveraging scaled in-house pipelines • Architect, build, and deploy automated analysis pipelines for diagnostic tests • Engineer novel genomic analysis tools and proactively identify optimization pathways • Participate in code reviews, technical documentation • Coordinate directly with downstream infrastructure teams to ensure R&D tools scale efficiently into production systems

• Serve as the field-based external facing medical representation of Medical Affairs • Create awareness of Ascendis Pharma in the endocrinology community and communicate the potential of TransCon technology to transform the practice of endocrinology • Maintain high level of medical expertise to support the portfolio/pipeline and relevant disease states (e.g., bone and growth) • Provide medical/scientific presentations to both internal and external audiences • Identify key opinion leaders (KOLs) and key organizations (e.g. professional associations, patient advocacy groups) for disease states within a geography • Identify the scientific needs of healthcare providers (HCPs), researchers, and patient advocates important to patient care within a geography • Develop and maintain a KOL engagement plan that foster collaborative relationships within geography • Capture external insights about the disease state, Ascendis portfolio and pipeline, and competitors and communicate to internal stakeholders in a timely and effective manner • Build strong relationships with internal colleagues (e.g., Market Access, Marketing, and Sales) by providing medical expertise and support as needed • Collaborate with Medical Outcomes Scientific Liaisons (MOSLs) to support regional deliverables (e.g., scientific support, internal/external presentations) • Participate with the development and implementation of the Field Medical Team strategic goals and objectives • Provide scientific support at medical congresses to include participation in clinical data presentations, scientific exchange at the medical affairs booth, and internal or external meetings • Provide internal onboarding and ongoing medical training for commercial and medical colleagues • Engage with external researchers as a primary contact with interest in investigator-initiated trials (IITs) • Support clinical trial operations to ensure success with planned and ongoing clinical trials to include identifying, supporting, and regularly engaging clinical trial investigators, and sites. Participate in patient find activities as needed. • Document all relevant activities in the CRM platform • Ensure understanding of and maintains compliance with department and corporate policies and procedures