• Responsible for performing concurrent reviews of patient records to ensure complete, accurate, and specific clinical documentation. • Should have a comprehensive understanding of ICD and CPT Coding Guidelines. • Responsible for clarifying conflicting, incomplete, or imprecise documentation by actively seeking answers and actively educating providers. • Work to continuously improve clinical documentation to best reflect the care provided and corresponding reimbursement. • Responsible for improving the overall quality and completeness of clinical documentation. • Facilitate modifications to clinical documentation through extensive concurrent interaction with physicians, nursing staff, other patient caregivers, and Coding staff to support that appropriate reimbursement, clinical severity of illness, and risk of mortality is captured for the level of service rendered to all patients. • Supports timely, accurate and complete documentation of clinical information used for measuring and reporting physician and practice outcomes. • Educates all members of the patient care team on an ongoing basis.

• The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. • Organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonization (ICH) and other regulatory guidelines, and individual company document standards. • Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regulatory documents. • Lead a project team, and actively participate in development and writing of high-quality documents (study-level and submission level documents, pharmacovigilance documents). • Author documents per client specifications, templates, style guides, and other guidance documents. • Author documents per regulatory authority guidelines and requirements. • Act as client advisor, working collaboratively and developing a strong relationship of trust built upon consistent and reliable communication; communicate ideas and strategies to produce a successful end result. • Practice blameless problem solving, taking broad perspectives in resolving issues to prevent negative impact to work. • Manage budget for a low complexity project, including all contributors (writers, editors). • Usher documents through the review process, conduct comment resolutions meetings (CRMs) and successfully lead a project team to consensus. • Maintain collaborative, proactive, and effective communication with both clients and internal teams. • Lead project-related meetings and teleconferences. • Provide coaching to junior staff for study level documents as well as submission level documents and ensure all staff comply with company standard operating procedures (SOPs) and training requirements.

• Lead ambitious initiatives that craft the future of clinical research • Deliver flawless Regulatory Medical Writing documents, such as protocols, CSR, and Investigator Brochures • Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies • Review routine documents prepared by junior team members and may provide training and mentorship for junior writers • Ensure compliance with quality processes and requirements for assigned documents • Provide input on and independently develop best practices, methods and techniques for achieving optimal results • Assist in program management activities including developing timelines, budgets, forecasts and contract modifications

Role Description As a CDI Coding Specialist, you ensure our documentation accurately reflects the complexity of the seniors we serve. Your work strengthens clinical accuracy, supports high‑quality care, and helps providers deliver the right care at the right time. This role is fast‑paced, detail‑driven, and deeply collaborative. You’ll review charts, validate documentation, and partner with providers to uphold the highest standards of coding excellence. If you thrive in a mission‑driven environment that values teamwork, integrity, and accountability, you’ll feel right at home here. Location: Remote within the U.S.; preference for those located in Eastern or Central time zones. Office Hours: Monday–Friday, 8am–5pm What You’ll Do - Master the chart, start to finish - Apply expert coding judgment using ICD‑10 guidelines to validate accurate diagnosis codes in medical record documentation - Support the clinical care teams through completion of comprehensive pre-visit and post-encounter chart reviews - Review documentation to ensure every submitted code is fully supported - Abstract relevant clinical information and diagnostic codes from hospital claims, radiology reports, and specialist notes - Strengthen documentation accuracy - Analyze MRA reports to surface unreported or unresolved conditions - Query providers when clarification or additional documentation is needed - Educate clinicians on HCC coding and documentation best practices - Maintain compliance and protect patient confidentiality - Keep data clean and workflows tight - Review system‑generated reports to correct or complete missing data - Communicate audit findings clearly and constructively to providers and internal teams - Collaborate across teams to ensure seamless workflows and shared accountability - Support timely amendments through ongoing review and query processes - Improve the work over time - Identify process gaps and recommend solutions - Enhance coding knowledge through continuous learning - Contribute to special projects and departmental initiatives as assigned - Participate in team meetings to stay aligned and drive improvement What Success Looks Like - Chart review accuracy consistently at 95%+ - Chart review production standards will be maintained with precision and efficiency - Clear, timely communication with providers and internal stakeholders - Strong alignment with coding guidelines, compliance standards, and organizational goals - Meaningful contributions to documentation quality and risk adjustment performance Qualifications - Professional Coder (CPC) Certification - 3+ years of experience in CMS-HCC risk adjustment or HCC coding - 3+ years of ICD‑10 coding experience - 1+ year of HEDIS/Stars experience - Experience working in both prospective and concurrent workflows - Strong knowledge of medical terminology, anatomy, physiology, disease processes, and pharmacology - Proficiency with MS Office (Excel, PowerPoint, Word) - Clear, professional communication and the ability to defend coding decisions - Strong organization, attention to detail, and comfort working in a fast‑paced, evolving environment - A mindset grounded in our core values: Heart, Excellence, Accountability, Resilience, and Teamwork Requirements - You hold a Certified Risk Adjustment Coder (CRC) credential - You have previous MRA experience supporting a primary care practice - You have experience educating providers on HCC coding and documentation - You proactively identify documentation gaps and recommend improvements - You thrive in collaborative, mission‑driven teams and look for ways to strengthen workflows Benefits - $33-$36 per hour, based on experience and qualifications - Generous annual performance bonus - Health, dental, and vision insurance - Paid time off + paid sick time - 401(k) with company match