• Performs initial case reviews and an appropriate number of follow-up reviews based on program standards. Uses clinical insight and judgment of clinical findings to assess clinical documentation for improvement opportunities. Independently develops complex queries. • Maintains query rate, response rate, and agreement rate in line with established performance benchmarks. • Assists with reviewing records at different Inova hospitals as needed and under the supervision of assigned CDI leaders. • Participates in all department-wide CDI and coding education on ICD-10, MS-DRG, and quality outcome measures as well as compliance requirements related to query (AHIMA Practice brief). • Maintains competency in the use of CDI applications to process daily work lists and report results of record reviews and queries. • Enters all required data into CDI applications to enable Coding professionals and Coding Quality Coordinators to determine the disposition of concurrent queries in order to assign the final MS-DRG as well as APR-DRG, SOI, and ROM and risk adjustment factors. • Demonstrates expert knowledge of ICD 10 codes and MS-DRG/APR DRG assignments. • Interacts with Coding Quality Coordinators and Coding professionals on any questions related to CDI working DRG related to concurrent queries and final coding. • Assists with any post-discharge (retrospective) queries per CDI policy/procedure and as requested by CDI leadership. • Demonstrates advanced technical ability with current software used by the department. • Provides electronic support to providers regarding best practice documentation standards and the query process. Provides 1:1 provider education within the daily workflow and participates in group education sessions as requested by CDI Leadership. • Participates in special projects, audits, and other duties as directed by CDI Leadership. May assist with precepting and education of new staff. • Works collaboratively with medical, nursing, and ancillary staff to improve the quality of chart documentation that assures appropriate DRG classification to accurately reflect patient severity of illness and risk of mortality. • Participates, and takes a leadership role in, select special projects, audits, and other duties as directed by CDI Leadership. • As needed, may travel across the Washington DC metro area to engage with providers. • May perform additional duties as assigned.

• Preparation of PMCF, CER, CEP, PMS. • Review of relevant documents. • Consultation and gap analysis on transition from MDD to MDR. • Responses to queries from regulatory authorities. • Perform literature search. • Appraise literature search data. • Ability to interpret, evaluate, and translate medical research findings.

Role Description We are seeking a Freelancer Senior Medical Writer, experienced with medical devices for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. The position is fully remote and the candidates can be based in every EU country or Armenia. - Preparation of PMCF, CER, CEP, PMS. - Review of relevant documents. - Consultation and gap analysis on transition from MDD to MDR. - Responses to queries from regulatory authorities. - Perform literature search. - Appraise literature search data. - Ability to interpret, evaluate, and translate medical research findings. Qualifications - Degree in Life Sciences. - At least 4-5 years of experience in medical writing. - Experience in medical device-related documents (CEP/CER/PMCF/PSP). - Fluent in English. - Knowledge of French language is a plus. - Submissions to FDA is a plus (for medical devices). - Regulatory consultation is a plus. Benefits - High-impact projects that nurture your potential. - Space to shine and push boundaries. - Becoming a key part of something bigger.

Role Description We are seeking a Freelancer Senior Medical Writer, experienced with medical devices for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. The position is fully remote and the candidates can be based in every EU country or Armenia. - Preparation of PMCF, CER, CEP, PMS. - Review of relevant documents. - Consultation and gap analysis on transition from MDD to MDR. - Responses to queries from regulatory authorities. - Perform literature search. - Appraise literature search data. - Ability to interpret, evaluate, and translate medical research findings. Qualifications - Degree in Life Sciences. - At least 4-5 years of experience in medical writing. - Experience in medical device-related documents (CEP/CER/PMCF/PSP). - Fluent in English. - Knowledge of French language is a plus. - Submissions to FDA is a plus (for medical devices). - Regulatory consultation is a plus. Benefits At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.