• Review, analyze, and summarize large volumes of medical records for peer review cases • Extract key clinical findings, diagnoses, treatment history, medications, procedures, provider notes, and timelines • Organize complex medical information into concise and accurate summaries • Support Independent Review Organization (IRO) workflows and peer review processes • Prepare documentation and case summaries for physician reviewers • Collaborate with providers and reviewers as needed to ensure complete documentation • Provide nursing home scribing and clinical documentation support when needed • Review orders, vital signs, and patient information within nursing home EHR systems • Maintain HIPAA compliance and confidentiality when handling patient records • Adapt quickly to new technologies and evolving workflows

Role Description Our client is seeking a highly analytical, detail-oriented, and clinically knowledgeable Clinical Documentation Specialist to support medical record review, peer review preparation, and healthcare documentation workflows. This role is ideal for candidates with a strong healthcare or clinical background who are comfortable reviewing complex medical records, understanding medical terminology, and extracting critical information from patient documentation. The Clinical Documentation Specialist will play a key role in supporting peer review cases by organizing, summarizing, and presenting relevant clinical information in a clear and accurate manner. In addition to peer review support, the role may include nursing home documentation and scribing responsibilities, requiring the ability to work across multiple EHR and EMR platforms while maintaining exceptional attention to detail and HIPAA compliance. This is an excellent opportunity for a healthcare professional seeking a specialized role focused on clinical documentation, medical record analysis, and healthcare operations support. Qualifications - Medical or clinical background required - Nursing background strongly preferred - Experience working in healthcare, clinical operations, medical records, utilization review, medical scribing, case review, or related fields - Strong understanding of medical terminology, diagnoses, treatments, and clinical documentation Requirements - Review, analyze, and summarize large volumes of medical records for peer review cases - Extract key clinical findings, diagnoses, treatment history, medications, procedures, provider notes, and timelines - Organize complex medical information into concise and accurate summaries - Identify relevant documentation required for peer review evaluations - Maintain accuracy and consistency when reviewing extensive medical records - Support Independent Review Organization (IRO) workflows and peer review processes - Prepare documentation and case summaries for physician reviewers - Assist with organizing records and supporting materials across peer review platforms - Help improve efficiency and turnaround times for case reviews - Collaborate with providers and reviewers as needed to ensure complete documentation - Provide nursing home scribing and clinical documentation support when needed - Assist with note-taking and documentation related to medical director responsibilities - Support chart review, clinical records management, and documentation workflows - Review orders, vital signs, and patient information within nursing home EHR systems - Navigate multiple healthcare platforms and documentation systems - Accurately enter, review, and organize patient information - Maintain HIPAA compliance and confidentiality when handling patient records - Adapt quickly to new technologies and evolving workflows Benefits - Access to world-class support for questions, guidance, contract matters, and client communication - Premium VPN Access (Optional): A secure VPN license can be provided upon request - HIPAA & Cybersecurity Training + Certification (Provided) - Top 1% VA Performance Training - Client-Approved U.S. Holidays - Client-Approved Paid or Unpaid Time Off - Access to Tools & Resources - Optional Performance-Based Incentives

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