• Lead the tactical execution of publications stemming from our global medical affairs publication plans • Develop strategic, high-impact scientific publications and congress materials in oncology • Collaborate with cross-functional teams and external experts in a biotech or pharmaceutical setting • Ensure data are communicated with clarity, accuracy, and impact through high-quality publications and congress materials • Establish and maintain professional relationships with internal colleagues, external authors, journal editors, publishers, and other professional bodies

• Create high quality scientific communications content to support internal and external data dissemination projects* • Play a key role in ensuring scientific communication deliverables are completed in a timely manner with stakeholder satisfaction* • Meet project milestones and escalate challenges as needed to ensure projects remain on track* • Critically evaluate data and translate information into succinct, scientific summaries* • Works cross-functionally with the broader clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met efficiently and effectively • Work with clinical study management and stats to create timelines for completing data dissemination plans related to clinical studies* • Prepare regular project status updates to management* • Prepare and/or edit manuscripts for submission to peer-reviewed journals and publication* • Prepare abstracts and presentations for submission and presentation at scientific conferences* • Conduct literature searches for devices and relevant disease states* • Keep current with literature for relevant disease states and supports maintenance of the clinical literature library* • Play critical role in supporting and developing scientific communication data dissemination strategy (ex. Journal identification, conference impact, potential sub- analysis, etc.) • Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. * • Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company. * • Ensure other members of the department follow the QMS, regulations, standards, and procedures. * • Perform other work-related duties as assigned.

• Develop and write high-quality scientific and medical content, including congress abstracts, posters, presentations and peer-reviewed original research articles and clinical studies. • Coordinate manuscript submissions, draft reviewer response documents, and revise and resubmit manuscripts and relevant supplementary materials to peer-reviewed journals. • Collaborate with cross-functional teams on manuscripts, including researchers, clinicians, and regulatory affairs, to ensure accuracy of scientific content and compliance with industry standards. • Conduct thorough literature reviews and stay updated on the latest advancements in genetics and genomics. • Translate complex scientific information into clear and accessible language for diverse audiences, including collaborators and management. • Ensure all written materials adhere to company guidelines, regulatory requirements, and best practices in medical writing (e.g. ICMJE and GPP best-practice guidelines). • Participate in the development and review of standard operating procedures (SOPs) related to medical writing and publication development activities. • Coordinate the Medical, Legal, and Regulatory review process for publications (publication review committee; PRC) in JIRA.

• Assist the providers with accurately identifying and documenting the healthcare services provided to the patient. • Analyze clinical information, using the documentation as the primary driver for overall System Case Mix Index. • Evaluate the documentation in order to assign the principal diagnosis, relevant secondary diagnoses, and procedures for accurate DRG assignment, risk of mortality, severity of illness. • Formulate queries when there is missing documentation, conflicting documentation or unclear documentation. • Provide ongoing education to physicians and essential healthcare providers regarding clinical documentation improvement. • Collaborate with nursing staff, clinical nutrition, pharmacists, along with the physicians on documentation. • Maintain the confidentiality of all information acquired pertaining to the patient, physician, associates, and visitors.