Foreclosure Title Reviewer Fully Remote • Columbia, SC • Title Job Type Full-time Description McMichael Taylor Gray, LLC is seeking Title Reviewers for states in our legal footprint. Candidates MUST HIGHLIGHT SPECIFIC EXPERIENCE AND LIVE in South Carolina. The ideal applicant will have experience in default operations, in Title Review and Title Curative matters. Requirements - Analyzing title documents and legal descriptions of the property. - Experience with navigating and researching online county records - Ability to manage multiple tasks simultaneously, prioritize and meet deadlines under pressure - Self-motivated, goal-oriented with a strong desire to succeed - Strong communication skills (verbal, written, and listening) - Ability to compose a professional email and concisely communicate title issues within a client case management platform - Possesses the ability to critically think about complex title issues Preferred Qualifications: - 3 years of title review experience required - Experience with the scope of Foreclosure and how it directly relates to Title preferred - Ability to input and/or verify a significant amount of data entry proficiently and with a high level of accuracy - Comfortable with applying decisive judgment with minimal supervision - Capable of examining and/or comparing county Tax/GIS maps, liens, judgments, leases, Deeds, agreements, Security Instruments, contracts, surveys, and plat books to confirm accurate legal descriptions and ownership thereof - Comfortable with Testate/Intestate succession and reviewing Probate documents within the chain of title to verify all interests are accounted for - Able to identify and input all parties requiring notice of Foreclosure (Non-Judicial or Judicial) into a case management platform - Proficient in explaining chain of title issues, priority issues, statute of limitations issues, missing assignments, legal description issues, etc. to clients clearly and concisely - Recognize title defects and formulate curative solution - Comfortable with reviewing Gap/Updated title reports with accompanying supporting documentation and confirming all parties were included in the Foreclosure proceedings - Familiar with Foreclosure Servicing platforms such as Black Knight, Tempo, etc. - Capable of identifying Mobile Homes and understanding how to de-title them appropriately for government conveyance - Proficient in locating obituaries online and skip tracing Heirs identified within - Comfortable with communicating with Tax offices, 911 addressing offices, Probate offices, Deed record offices, etc. to obtain needed information - Able to maintain production levels on a daily basis Skills/Abilities: - Notaries or candidates willing to become a notary preferred. - Ability to prioritize numerous tasks in a high-volume environment - Excellent customer service skills including professional conduct in communicating with Attorneys, Co-Workers, and Clients - Ability to work both independently and as part of a team - Technologically proficient with MS Office Suite, specifically MS Outlook, MS Word, and MS Excel, along with other electronic databases. (Excel - able to add/delete rows and columns, sort and filter, search for data within a workbook and other basic formatting) - Proficiency with operating in a digital document environment We offer a competitive benefits package and compensation is commensurate with experience.

Title: Data Reviewer - GMP Labs (PCC) Location: Remote Wisconsin United States of America Details: Fully remote, full time Department: Physical Chemistry and Characterization This is a fully remote role supporting our GMP Lab in Middleton, Wisconsin. We welcome applicants from all locations within the US. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Discover Impactful Work: The Data Reviewer performs review of a variety of routine and complex analytical analysis experiments that are conducted on pharmaceutical and biopharmaceutical compounds with various formulations and/or biological matrices. Ensures analyses are following validated or experimental analytical procedures, and compare results to methodology, protocol and product specifications, Standard Operating Procedures (SOPs) acceptance criteria, and Good Manufacturing Practices (GMP). Reviews data entered into databases and reports and monitors the quality of the laboratory data. Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis review independently. A Day in the Life: - Evaluates laboratory data for compliance with analytical methods, client directives, and SOPs. - Reviews sample results for scientific soundness, completeness, accurate representation of the data, and final reported results. - Communicates with laboratory staff to proactively maintain the quality of laboratory documentation. - Delivers review findings noting deficiencies within the analytical data or reports in a clear and concise manner. - Escalate significant deficiencies to the project leader or supervisor for assessment. - Facilitates in conversations with lab staff on best documentation practices and addressing quality findings. - Advocates for quality and review process changes. - Identifies and supports process improvement initiatives. - Performs other duties as assigned. Keys to Success: Education - Bachelor's degree or equivalent and relevant formal academic / vocational qualification Experience - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role Knowledge, Skills, Abilities - Familiarity with Karl Fischer (KF) and compendial methods (USP, Ph. Eur., JP, ChP) preferred - Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP - Thorough knowledge of chromatography. - To demonstrate behaviors which align to the 4i Values of Thermo Fisher - Strong technical knowledge including an understanding of laboratory procedures, methodology, and standards - Strong verbal and written communication skills - Strong attention to detail - Ability to balance time and remain focused on work to meet goals - Ability to train staff on basic review techniques - Ability to independently review laboratory reports and analytical methods - Ability to deal with multiple and changing priorities - Ability to provide clear and concise feedback and/or documentation of results - Ability to work in a collaborative team environment - Ability to work efficiently in a remote capacity

Role Description The Clinical and Coding Quality Supervisor provides direct operational leadership and subject matter oversight for all daily clinical and coding quality workflows and assignments. This role is responsible for ensuring the accuracy, consistency, and effectiveness of second-level coding quality review workflows that support: - Risk adjustment - DRG integrity - Regulatory compliance - Institutional quality and financial performance Promote and support teamwork and engagement, performance excellence, accountability, and professionalism. Lead and support process improvement. Ensure the Clinical & Coding Quality Team have the education and tools they need to successfully perform to the highest levels of quality and compliance. Qualifications - Associate's degree in nursing or health information management - 5 years of experience working in an Acute Hospital setting preferably in an Academic environment - 3 to 5 years’ experience working in a Quality/Risk Program - Experience utilizing methodology-specific risk calculators and guidance documents - Experience working in a remote environment - Registered Health Information Management (RHIA), Registered Nurse (RN) with Certified Clinical Documentation Specialist (CCDS), Registered Health Information Technology (RHIT), or AHIMA Certified Coding Specialist (CCS) Requirements - Bachelor's degree in nursing or health information management (preferred) Job Duties - Manages staffing and all employee related duties. - Provide day-to-day supervision of Coding Quality Analysts, including work assignment, prioritization, performance monitoring, and issue resolution. - Oversee all quality workflow and assignments: - Ensure quality changes are completed within revenue cycle goals and corrections are completed within deadlines. - Serve as the primary escalation point for complex CDI, coding, DRG, and risk-adjustment questions requiring advanced review. - Oversee coding quality audits validating ICD-10-CM/PCS code assignment accuracy, abstracted data accuracy, completion and implementation of coding audit recommendations. - Track, trend, and report quality metrics, including error rates, rework, and risk-adjustment performance to Leadership. - Identify front-end workflow issues impacting coding quality and recommend process improvements. - Collaborate with Denials Team processes and initiatives. - Maintains an expert level of knowledge of Coding, CDI, Denials, and Appeal guidelines and practices. - On-boards, trains, and audits new Coding Quality Analysts. - Support the Quality Standards set by UTSW & the Coding Quality & Integrity Department. - Other duties as assigned. Benefits - PPO medical plan, available day one at no cost for full-time employee-only coverage - 100% coverage for preventive healthcare - no copay - Paid Time Off, available day one - Retirement Programs through the Teacher Retirement System of Texas (TRS) - Paid Parental Leave Benefit - Wellness programs - Tuition Reimbursement - Public Service Loan Forgiveness (PSLF) Qualified Employer

Role Description We are sharing a specialised part-time consulting opportunity for physicians experienced in clinical diagnosis, treatment planning, patient care management, medical documentation, clinical compliance, and structured medical workflow review. This role supports current and upcoming remote consulting opportunities focused on medicine-related clinical review, diagnostic reasoning evaluation, patient care workflow assessment, medical documentation review, clinical output validation, and high-quality project execution. Selected professionals will apply their physician expertise to review realistic medical scenarios, evaluate clinical outputs, prepare structured written feedback, and support accurate, evidence-based healthcare workflow tasks. Key Responsibilities - Clinical Diagnosis & Treatment Review - Review medical scenarios involving clinical diagnosis, differential diagnosis, treatment planning, patient history, symptoms, and care decisions. - Evaluate clinical outputs against source materials, medical standards, patient context, and documented review criteria. - Support structured review of clinical notes, case summaries, diagnostic reasoning, treatment recommendations, and patient management workflows. - Identify missing clinical context, reasoning gaps, documentation issues, and expected physician review outcomes. - Patient Care Management & Medical Documentation - Review scenarios involving patient care management, follow-up planning, care coordination, clinical documentation, and compliance-related medical workflows. - Evaluate medical documentation for clarity, accuracy, completeness, and alignment with clinical expectations. - Support structured review of EHR-style notes, care plans, discharge summaries, patient summaries, and clinical communication materials. - Prepare clear written feedback based on source materials and verifiable clinical criteria. - Medical Evaluation & Structured Feedback - Review medicine-related tasks and deliverables based on real-world physician workflows. - Provide domain-specific feedback on clinical accuracy, patient safety, diagnostic reasoning, and communication quality. - Support evaluation workflows involving AI-generated clinical summaries, care recommendations, documentation outputs, and medical reasoning. - Maintain accuracy, consistency, and professional judgment across submitted work. Qualifications - Professional physician experience in clinical diagnosis, treatment planning, patient care management, medical documentation, compliance, or healthcare operations. - Background in one or more areas such as primary care, internal medicine, family medicine, hospital medicine, emergency medicine, specialty care, or clinical advisory work. - Familiarity with medical workflows involving patient assessment, diagnosis, treatment planning, documentation, follow-up care, and clinical compliance. - Comfort reading and preparing medical artifacts such as clinical notes, patient summaries, treatment plans, discharge materials, diagnostic explanations, and care documentation. - Strong written communication skills. - Ability to work independently in a remote, project-based environment. Requirements - MD, DO, or equivalent physician qualification is strongly preferred. - Active or prior medical licensure, board certification, board eligibility, residency training, or specialty training is highly relevant depending on project scope. - Clinical practice experience, medical teaching, healthcare quality work, or documentation review experience is also valuable. Nice to Have - Experience in hospital, clinic, academic medical center, telehealth, urgent care, primary care, specialty practice, or healthcare quality environments. - Familiarity with EHRs, clinical guidelines, medical documentation standards, patient safety workflows, care pathways, or compliance-related medical review. - Experience preparing or reviewing clinical notes, treatment plans, diagnostic summaries, patient cases, care recommendations, or medical review materials. - Interest in medical AI, clinical decision support, healthcare data quality, or clinical workflow evaluation. - Strong attention to detail in clinical, patient-facing, and documentation-heavy healthcare environments. Benefits - Apply physician expertise to structured remote clinical review work. - Contribute to high-quality medical workflow evaluation, diagnostic reasoning review, and healthcare documentation assessment. - Work on flexible assignments aligned with your clinical background. - Use your physician judgment in a focused, evidence-based review environment. - Remote structure with competitive hourly compensation. Contract Details - Independent contractor role. - Fully remote with flexible scheduling. - Part-time commitment depending on project availability. - Competitive rates between $150–$220 per hour depending on expertise. - Weekly payments via Stripe or Wise. - Projects may be extended, shortened, or adjusted depending on scope and performance. - Work will not involve access to confidential or proprietary information from any employer, client, or institution. About the Platform This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams. By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy .