• 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.

• Review inpatient medical records to identify documentation gaps and improvement opportunities • Craft physician queries that clarify diagnoses and procedures • Educate providers on documentation best practices and regulatory requirements • Monitor key metrics including CMI trends and query response rates • Support denial management with clinical justifications for appealed claims • Collaborate with coding teams for accurate DRG assignment • Develop documentation policies aligned with CIHQ accreditation standards

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description We are seeking a detail-oriented and highly organized Medical Scribe to join our team. This position supports remote work, providing the opportunity for flexible scheduling and the ability to work from the comfort of your own home. - Accurately and efficiently transcribe medical notes, procedures, and diagnoses into electronic medical records - Assist healthcare providers with documentation during patient appointments - Coordinate communication between healthcare providers and other medical staff - Maintain patient confidentiality and adhere to HIPAA guidelines - Ensure accuracy and completeness of medical records - Perform other administrative tasks as needed Qualifications - Previous experience working as a Medical Scribe or in a similar role - Knowledge of medical terminology and procedures - Strong typing and computer skills - Excellent communication and interpersonal skills - Ability to work independently and prioritize tasks effectively - Attention to detail and accuracy