• Major contributor to document authorship for a variety of documents across different service lines • Project lead on smaller projects, interfacing directly with the client • Support larger, more complex engagements as a member of a larger delivery team • Use expertise in clinical regulatory writing to lead teams and help clients achieve their goals

• Perform audits based on organizational priorities, including concurrent CDI workflows and retrospective auditing. • Conduct reviews that may lead to the addition, deletion, adjustment, or confirmation of diagnoses. • Initiate queries for documentation clarification to ensure the highest level of clinical accuracy. • Utilize and review AI tools and 'Human-in-the-Loop' outputs to support modern auditing processes. • Assist in creating and communicating provider and vendor education regarding trends and opportunities in compliant coding practices. • Collaborate with the CDI Manager to make recommendations that enhance coding quality goals and outcomes. • Remain current on ICD-10-CM coding guidelines, AHA Coding Clinic Guidance, and CMS Risk Adjustment guidance.

Role Description The goal of this position is to support all care teams across the region in comprehensive and targeted chart reviews -- to ultimately facilitate efficient and effective medical care for our patients. In addition, this role will partner with regional leaders, particularly the Population Health Director and Senior CIS, to indirectly support daily huddle and CDR workflow optimization. CDSs are trained to be experts in structured clinical assessments, accurate and specific documentation, population health workflows, and team-based care. - Chart Reviews - Access and review HIE/EMRs to identify potential suspects based on test results, etc. - Identify the need for Medical Records requests from Blue Button and other payer data - Prepare and lead monthly Rejected Suspect Reviews - Partnership with Population Health Director on general review support - Identify and analyze opportunities for improving patient quality outcomes and cost of care - Analyze chronic condition prevalence based on patient demographics and identify opportunities for interventions - Monitor clinical documentation efforts - Other duties, as assigned Qualifications - Ease and expertise working with multiple technical systems, including Greenway, Canopy, and Excel - Ability to collaborate across multiple teams and engage in multiple perspectives to work toward a common goal - Proven experience and ability to build relationships with Providers - Proficiency in tracking down and leveraging external resources, such as hospital records, Blue Button, and payer data, to support retrospective and prospective accurate documentation - Ability to succeed in a fast-paced, ever-changing environment - Self-starter with a high degree of drive, initiative, and follow through - Ability to develop, plan, and implement short and long term goals - Exceptional interpersonal, written and verbal communication skills - Commitment to company vision - Experience in accurate and specific documentation - U.S. work authorization - Someone who embodies being “Oaky” Requirements - Radiating positive energy - Assuming good intentions - Creating an unmatched patient experience - Driving clinical excellence - Taking ownership and delivering results - Being scrappy Benefits - Collaborative and energetic culture - Fast-paced and innovative environment - Competitive benefits including paid vacation and sick time - Generous 401K match with immediate vesting - Health benefits

• Take the lead role in projects where required and take ownership of the scientific/editorial component. • Responsible for producing high-quality scientific written materials in keeping with project briefs. • Assist with editing and proofreading of text written by other team members and provide constructive feedback to aid learning and development. • The role will involve reviewing and interpreting data from preclinical and clinical research articles as the basis of creating scientific written materials in keeping with project briefs. • Remains current with medical developments and conducts literature searches to ensure delivery of accurate medical information for assigned projects. • Participate in client meetings / teleconferences and attend scientific meetings as required. • Synthesizes clinical trial data and translates relevance for the appropriate physician and consumer audiences according to client requirements for assigned projects.