• Prepare high-quality abstracts and presentations for submission and presentation at conferences. • Engage in scientific writing and/or edit manuscripts for submission to peer-reviewed journals to achieve publication goals. • Ensure scientific communication deliverables are completed in a timely manner. • Evaluate data and translate information into succinct, scientific summaries. • Collaborate cross-functionally with clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met. • Work with clinical study management and statistics teams to create timelines for completing data dissemination plans related to clinical studies. • Strong communication with physician authors to achieve deliverables, maintain relationships, and to facilitate overall scientific communication efforts. • Contribute to the preparation of clinical data for analysis and scientific writing. • Conduct literature searches for relevant disease states and maintain the clinical literature library. • Lead cross-functional project reviews and serve as a core team member and subject matter expert on clinical study teams to create timelines for completing medical writing documents. • 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. *Indicates an essential function of the role