• You will generate content outlines that contain a clearly highlighted story arc and a complete reference list. • We will rely on you to develop client-ready drafts of content in various forms (slide decks, executive and comprehensive summaries, and other meeting materials). • We look forward to you organizing and annotating references in accordance with client’s directives or house style. • We anticipate you will confer with the teams in the medical/legal/regulatory (MLR) review process, answering all queries from the MLR review committee, and understand and implement the required changes.

• Responsible for concurrent review of inpatient medical records to identify opportunities for improving the quality of medical record documentation • Confer with the appropriate caregiver on the additional documentation that may be required • Achieve a complete medical record by the time of patient discharge • Follow Joint Commission, Medicare and third party payor documentation guidelines • Provide assistance to the attending physician and other health care providers in the patient care documentation process

• 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.