Role Description The Clinical Documentation Integrity Specialist (CDIS) facilitates the overall quality, completeness, and accuracy of clinical documentation through concurrent interaction with providers and other members of the healthcare team. The CDIS ensures that documentation accurately reflects the patient’s clinical conditions and level of service. The CDIS communicates with providers through discussion and/or compliant queries to address missing, unclear, conflicting, or clinically unsupported diagnoses. The role includes: - Appropriate assignment of MS-DRG/APR-DRG - Severity of illness (SOI) - Risk of mortality (ROM) - Identification of relevant clinical indicators (e.g., HACs, PSIs) The CDIS applies principles of clinical validation and ensures all queries comply with AHIMA/ACDIS guidelines and the CDI Code of Ethics. Qualifications - Bachelor's degree preferred - Minimum of one (1) year of inpatient coding experience and/or experience working as a Clinical Documentation Integrity Specialist in an acute care setting - Strong knowledge of MS-DRG, APR-DRG, ICD-10-CM/PCS coding guidelines - Experience using encoder and electronic health record (EHR) systems - Excellent verbal and written communication skills - Strong analytical thinking, problem-solving abilities, and attention to detail - Proficiency in Microsoft Office applications preferred Requirements - ACDIS Certified Clinical Documentation Specialist (CCDS) or AHIMA Certified Documentation Integrity Practitioner (CDIP) required within 1 year of hire/transfer Benefits - Delivering world-class health care one patient at a time Pay Range $69.00 - $69.00

Role Description We are seeking a Senior Regulatory Medical Writer to provide fractional, on-demand support for regulatory submission activities. This role focuses on independently updating and finalizing regulatory documents to support ongoing agency interactions and submission deliverables, working alongside internal and contract writers. - Independently update, revise, and finalize regulatory documents, including protocol and IB - Support preparation and maintenance of protocol amendments, submission support documents, and related deliverables within Common Technical Document (CTD Modules 2–5) across the submission lifecycle (responses, amendments, briefing packages) - Ensure scientific accuracy, clarity, consistency, and compliance across all regulatory documents - Collaborate with internal teams and contract writers to ensure timely delivery aligned with regulatory and quality standards - Support intermittent workload demands (~10–15 hours/week during active project periods) Qualifications - Regulatory medical writing experience supporting IND, CTA, NDA, and/or BLA submissions - Strong familiarity with Common Technical Document (CTD) structure and regulatory submission lifecycle (e.g., responses, amendments, briefing packages) - Ability to work independently with minimal oversight in a fast-paced, cross-functional environment - Strong attention to detail with demonstrated ability to ensure scientific and regulatory quality standards - Proven collaboration experience with regulatory, clinical, and medical writing teams

• Providing improvement in the overall quality and completeness of medical record documentation • Obtain appropriate clinical documentation through extensive interaction with physicians, nursing staff, other patient caregivers, and coding staff • Ensure proper reimbursement is received for the level of service rendered to patients • Educate members of the organization on documentation guidelines and improvement efforts

• Oversee strategies and planning for the CDI Program • Promote effective review of physician documentation • Collaborate with interdisciplinary teams • Provide ongoing Clinical Documentation management program education • Develop and manage departmental budgets