• The CDI Specialist is responsible for comprehensive secondary clinical chart reviews to identify potential missed opportunities for documentation clarification. • Collaborates closely with Coders, Coding Educators, Coding Quality Auditors, Case managers, Quality Department and Providers to assure documentation is clinically appropriate, accurately reflects the severity of illness and risk of mortality for the patient and is reflective of current CMS or other regulatory standards. • Conducts daily, concurrent review of inpatient records on assigned unit(s) to ensure complete and accurate physician and or clinician documentation is present at the time of discharge for accurate, timely, and compliant coding. • Reviews daily admissions to assigned unit, perform initial code assignment for a working DRG and complete CDI software data entry for initial and follows up case reviews (or worksheet to include code and DRG assignment) and submit to Program Assistant. • Updates “working DRG” as documentation supports, or physician query answer supports a change in the DRG assignment. • Communicates to the CDI Coordinator when volume of daily review assignments is too high or low so that CDI Coordinator can assist in adjusting review assignments amongst the team. • Initiates compliant physician queries when documentation is confusing, ambiguous, or missing and follows up with MD to seek immediate response to query.

• Develop high-quality medical and scientific content • Collaborate with internal stakeholders and external experts • Ensure content compliance with regulatory standards • Maintain up-to-date knowledge of therapeutic areas

• Develop high-quality medical and scientific content • Write clinical summaries and scientific manuscripts • Collaborate with medical affairs and regulatory teams • Ensure compliance with regulatory and ethical standards

• Develop scientifically accurate, compliant, and engaging content for pharmaceutical marketing initiatives. • Bridge scientific knowledge and commercial objectives to create impactful content for healthcare professionals (HCPs). • Develop, repurpose, and update content for a wide range of commercial and promotional assets. • Ensure all developed content complies with applicable local regulations, industry standards, client requirements, and internal compliance policies, supported by accurate and up-to-date scientific references. • Manage content through the medical, legal, and regulatory (MLR) review and approval process, including addressing reviewer feedback and implementing required revisions. • Collaborate with cross-functional internal teams involved in end-to-end asset development, including creative, editorial, and digital production teams. • Coordinate with external stakeholders such as program managers, delivery managers, agency partners, and brand teams as needed. • Demonstrate openness and adaptability in using AI-enabled tools and digital platforms that support content development and operational efficiency. • Maintain compliance with quality standards, timelines, confidentiality requirements, data security protocols, training requirements, and established operational processes and policies.