Role Description We are sharing a specialised part-time consulting opportunity for professionals experienced in clinical documentation, medical scribing, CDI workflows, encounter notes, discharge summaries, EHR documentation, and structured healthcare documentation review. This role supports current and upcoming remote consulting opportunities focused on structured clinical documentation review, encounter note analysis, transitions-of-care documentation, CDI query assessment, EHR workflow review, and high-quality project execution. Selected professionals will apply their clinical documentation expertise to review realistic healthcare scenarios, evaluate documentation requirements, prepare structured written outputs, and support accurate, evidence-based clinical documentation tasks. Key Responsibilities - Encounter Documentation Review - Review clinical documentation scenarios involving SOAP notes, H&Ps, progress notes, encounter summaries, and source-supported clinical findings. - Evaluate encounter documentation against required elements, source materials, clinical note structure, and documentation standards. - Support structured review of patient history, exam findings, assessment details, plans, and progress documentation. - Identify missing elements, unsupported findings, documentation gaps, and expected clinical note outcomes. - Transitions of Care & Medication Documentation - Review discharge summaries, transitions-of-care materials, medication reconciliation records, and required-field documentation. - Evaluate discharge documentation against source materials, medication lists, care instructions, follow-up requirements, and documentation criteria. - Support structured review of clinical summaries, medication reconciliation details, handoff materials, and continuity-of-care documentation. - Prepare clear written explanations for documentation decisions based on provided materials and verifiable criteria. - CDI Query & EHR Workflow Support - Review CDI query scenarios involving documentation gaps, query framing, rule-based triggers, and clinical clarification workflows. - Evaluate CDI queries against documented facts, required wording standards, clinical context, and structured review criteria. - Support structured review of EHR documentation workflows using systems such as Epic, Cerner, or similar platforms. - Maintain accuracy, consistency, and professional judgment across submitted work. Qualifications - 2+ years of experience as a medical scribe, CDI specialist, RN, NP, PA, clinical documentation specialist, medical records reviewer, or similar documentation-heavy healthcare professional. - Experience with one or more areas such as SOAP note preparation, H&P documentation, progress notes, discharge summaries, CDI query practice, medication reconciliation, or EHR documentation workflows. - Familiarity with EHR systems such as Epic, Cerner, Meditech, Athenahealth, eClinicalWorks, or similar healthcare documentation platforms. - Comfort reading and preparing clinical artifacts such as SOAP notes, H&Ps, progress notes, discharge summaries, CDI queries, encounter summaries, and medication reconciliation records. - Strong written communication skills and ability to explain clinical documentation reasoning clearly. - Ability to follow structured instructions and produce evidence-based work. Requirements - A degree or professional background in nursing, medicine, physician assistant studies, health information management, clinical documentation, medical assisting, healthcare administration, or a related field is helpful. - Equivalent practical experience in medical scribing, CDI work, clinical documentation review, medical records review, or EHR documentation workflows is also highly relevant. Benefits - Apply clinical documentation expertise to structured remote project work. - Contribute to high-quality encounter note review, discharge documentation assessment, CDI query analysis, and EHR workflow support. - Work on flexible, project-based assignments aligned with your professional background. - Use your clinical documentation judgment in a focused, detail-oriented consulting 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 $60–$90 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.

• Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. • Leads the resolution of comments from the client. • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. • Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. • Coordinates quality and editorial reviews. • Ensures source documentation is managed appropriately. • Leads team document reviews, and reviews documents as needed. • Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format. • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. • Provides feedback to further define statistical output required and document needs. • Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. • Performs online clinical literature searches and complies with copyright requirements. • Identifies and proposes solutions to resolve issues, escalating as appropriate. • Provides technical support, training, and consultation to department and other company staff. • May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities. • Mentors and leads less experienced medical writers on complex projects, as necessary. • Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. • Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. • Completes required administrative tasks within the specified timeframes. • Performs other work-related duties as assigned. • Minimal travel may be required (less than 25%).

- Author and edit clinical documents, including Clinical Evaluation Reports (CERs), literature reviews, and regulatory submissions. - Plan and report clinical data collection for PMCF and clinical trials nationally and internationally. - Ensure clinical documentation compliance with EU MDR, FDA, and other international regulatory requirements. - Collaborate with Global Regulatory & Clinical Affairs teams to maintain clinical documentation within the Quality Management System. - Stay updated on scientific literature and regulatory changes within the company’s therapeutic area. - Participate in cross-functional projects and contribute to clinical strategy and documentation planning. - Support Medical Affairs for literature reviews and writing of documentation

Improve the accuracy and completeness of clinical documentation in outpatient records, collaborate with healthcare providers for optimal coding, and ensure compliance with guidelines to enhance risk capture and reimbursement.