Role Description LE DEPARTEMENT DE LA DORDOGNE RECRUTE PAR VOIE CONTRACTUELLE UN EDUCATEUR AIDE EDUCATIVE A DOMICILE (H/F) SPECIALITE EDUCATEUR SPECIALISE A LA DIRECTION GENERALE ADJOINTE DE LA SOLIDARITE ET DE LA PREVENTION- SECTEUR SARLAT. EMPLOI TEMPORAIRE DE 3 MOIS A TEMPS COMPLET Régime A.R.T.T. : Cadre général de l’organisation Missions : Au regard des compétences du Conseil Départemental mises en œuvre par l’Unité Territoriale, l’éducateur(trice) AED propose un accompagnement individualisé aux familles, afin de répondre à leurs besoins d’aide éducative. Il s’agit d’accompagner les familles vers une amélioration de leur situation. Il est en responsabilité de la protection de l’enfance. - Accompagner la situation individuelle, familiale et sociale des mineurs et jeunes majeurs relevant de l’aide sociale à l’Enfance dans le cadre de l’action éducative à domicile - Mener des actions éducatives dans le but de favoriser l’intégration des bénéficiaires et de leurs familles dans la vie sociale - Suivre l’évolution de chaque projet éducatif, évaluer les actions contenues et y apporter éventuellement des aménagements - Réaliser des écrits professionnels rendant compte des prises en charge réalisées et proposant des projets éducatifs et un plan d’aide. - Investir les temps d’analyse des situations (synthèses…) - S’impliquer dans le travail en transversalité avec les assistants sociaux de polyvalence de secteur, les référents insertion et les partenaires (Adsea, Mission Locale…) - Favoriser la restauration des liens avec la famille et l’environnement social. - Participer aux audiences chez le Juge des Enfants pour les situations qui sont confiées au service - Participer aux actions collectives du territoire (LAEP…) - Créer une relation éducative personnalisée en utilisant différents supports (actes de la vie quotidienne, activités de loisirs, de travail) Qualifications - Diplôme d'Etat d’Educateur Spécialisé exigé (DEES) - Connaissances en sciences humaines et droit - Connaissances et respect des lois et réglementations sociales, notamment celles de la protection de l’enfance - Connaissance et application des politiques en faveur de la jeunesse - Maitrise des techniques d’écoute, de relations bilatérales et d’animation socio-éducative - Maitrise des techniques de communication écrites et verbales - Respect du secret professionnel - Savoir piloter des projets éducatifs et aide à la décision - Travailler en équipes pluridisciplinaires et partenariales variées - Savoir réagir à des situations d’urgence, de conflit ou d’agressivité Qualities - Ecoute - Autonomie - Aptitude au travail en équipe - Force de proposition - Conduite d’entretien - Disponibilité - Empathie - Initiative - Sens de l’écoute - Savoir se distancier - Sens du contact - Savoir organiser son temps de travail - Capacités d’adaptation à des situations diverses

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals. At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees. With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive. We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career! Senior Regulatory Medical Writer The Senior Regulatory Medical Writer will collaborate with internal teams to lead, write, and manage completion of clinical regulatory documents. This role is for an individual contributor, reporting to the Executive Director (Head) of Regulatory and Medical Writing. This role includes responsibilities throughout the lifecycle of a document including working cross-functionally to interpret source information (including leading data interpretation meetings), leading key messaging meetings, writing content following US and international regulations (including Marketing Application Module 2 summary documents), conducting quality control (QC) reviews, resolving Quality Assurance (QA) audit findings, and working with Regulatory Operations for publishing and submission. This role reports to the Executive Director (Head) of Regulatory and Medical Writing. This position may be fully remote; however, preference will be given to San Diego-based applicants. RESPONSIBILITIES: - Working with the Executive Director, Regulatory and Medical Writing, collaborate with internal teams (e.g., Clinical Development and Biostatistics) to lead and/or contribute to the writing and management of clinical regulatory documents (e.g., clinical study reports, marketing application summary documents [Module 2], Investigator’s Brochures, clinical study protocols, briefing documents, etc.). - Coordinate the review cycles for documents; schedule and lead and/or contribute to data interpretation meetings, comment resolution meetings, and other document-related meetings. - Responsible for planning (in collaboration with Global Project Management) and meeting timelines for deliverables. - Understand, assimilate, and interpret sources of information with appropriate guidance. - Ensure compliance with appropriate conventions, proper grammar usage, and correct format requirements, as needed (e.g., formatting, hyperlinking). - Perform QC reviews as necessary. - Interact with Quality Assurance (QA) to resolve audit findings for specific documents. - Serve as Medical Writing department representative on project/core teams. - Lead/contribute to key messaging/storyboarding cross-functional meetings, ensuring the messages are clear and consistent within and across documents. - Maintain expert knowledge of US and international regulations, requirements, and guidance associated with preparation of regulatory documentation. - Effectively coordinate with Regulatory Operations to ensure on-time preparation and publication of regulatory submission documents. - Support Global Regulatory Lead with preparing information/responses requested by regulatory agencies. - Other duties as assigned. REQUIREMENTS: - Bachelor’s Degree required, advanced degree a plus. - A minimum of 5 years of direct experience as a medical writer preparing regulated documents in the pharmaceutical industry. Drug marketing application experience preferred. Rare disease experience is a plus. - Experience writing, as lead and/or contributor, important regulatory and clinical documents such as clinical study reports (all sections including safety narratives), Investigator’s Brochures, clinical study protocols, drug marketing application summary documents, Investigational New Drug applications, clinical sections of New Drug Applications, and other regulatory documents (e.g., Briefing Documents) for submission. Experience in writing Safety sections of regulatory documents preferred. - Solid working knowledge of relevant FDA, EMA, and ICH guidelines, particularly ICH E3 and ICH E6(R3). - Deep understanding of the drug development process. - Strong ability to assimilate and analytically interpret scientific data. Experience preparing data tables and basic figures. - Proficient knowledge of American Medical Association (AMA) style guidelines. - Ability to find and correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy. - Excellent attention to detail in writing, editing, formatting, and document QC. - Excellent time-management skills. Ability to balance multiple projects simultaneously. - Technical proficiency with Microsoft Office and Adobe Acrobat, and document management systems such as Veeva. - Experience with StartingPoint templates preferred. - Ability to follow style guides, lexicons, and eCTD templates etc. - Excellent written, oral (including presentations), and project management skills. - Energetic, self-motivated, and a hands-on professional with a strong work ethic. - Ability to be productive and work collaboratively in a dynamic, intense, and fast-paced environment. - Desire and ability to be a true team player working toward common goals. - Willing to ask for help when needed. A brief medical writing exercise may be requested at time of interview. Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition #IONIS004004 Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits The pay scale for this position is $113,000 - $142,426 NO PHONE CALLS PLEASE. PRINCIPALS ONLY. Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

Overview Performs inpatient chart review to determine appropriate DRG assignment and assures appropriate documentation in the chart to support clinical care provided, including severity of illness and risk of mortality which impacts Case Mix Index and mortality ratings. Coordinates with physicians, nurses, ancillary staff, and the coders in Health Information Management to identify and record principal and secondary diagnoses, principal procedures, and assign the working DRG. Performs second level review of specific DRGs as assigned. Presents education related to CDI topics to peers and providers we needed or requested. Reviews DRG denials and provides information to the denials team related to appealing the encounter Qualifications Certifications: Registered Health Information Administrator (RHIA) - American Health Information Management Association (AHIMA)American Health Information Management Association (AHIMA); Licensed Registered Professional Nurse (RN) - Illinois Department of Financial and Professional Regulation (IDFPR)Illinois Department of Financial and Professional Regulation (IDFPR), Education: Associate's Degree: Related Field, Work Experience: Clinical bedside; CDI Responsibilities Conducts the initial concurrent review process for all selected admissions. Clarifies documentation in the medical record as appropriate through communication with the physicians, nurses, and ancillary staff. Assures documentation in chart represents a true clinical picture of the patient diagnoses and supports care that was given and DRG assigned. Documents findings within Carle CDI software and updates software as required to reflect status of the encounter and any follow up. Coordinates with the physicians, nurses, ancillary hospital staff, and Health Information Management Department's coding staff to identify and record principal and secondary diagnoses, principal procedures, and assign the working DRG. Follows query process and escalates as necessary. Conducts education related to CDI topics to peers and providers as needed or requested. Performs second level review on selected inpatient encounters. Reviews denials for accurate and complete documentation and develops appeal letter when needed. Attends mandatory and regular education sessions as needed. Follows appropriate workflow in EPIC and CDI software and notifies one up leader of any issues. May serve as an "expert" and participate in testing for upgrades as needed. About Us Find it here. Discover the job, the career, the purpose you were meant for. At Carle Health, we're committed to fostering a workplace where every team member feels valued, respected and empowered, where passion and purpose come together to positively impact the lives of our patients and our communities. Find it all at Carle Health. Our nearly 17,000 team members and providers work together to support patient care across central and southeastern Illinois. We’ve grown to include eight, award-winning hospitals and a multispecialty provider group with more than 1,500 doctors and advanced practice providers. We’re developing the next generation of providers and healthcare professionals through Carle Illinois College of Medicine, the world’s first engineering-based medical school, and Methodist College. Carle BroMenn Medical Center, Carle Foundation Hospital, Carle Health Methodist Hospital, Carle Health Proctor Hospital, Carle Health Pekin Hospital, and Carle Hoopeston Regional Health Center hold Magnet® designations, the nation’s highest honor for nursing care. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Carle Health participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. | For more information: human.resources@carle.com. Compensation and Benefits The compensation range for this position is $34.31per hour - $59.01per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including, but not limited to, the candidate’s experience, qualifications, location, training, licenses, shifts worked and compensation model. Carle Health offers a comprehensive benefits package for team members and providers. To learn more visit careers.carlehealth.org/benefits.

• Lead a team of up to 8 CDSs • Ongoing audits and feedback for CDSs in pod • Routine 1:1s • Point person for suspecting questions from CDSs within their pod • Conduct bi-weekly pod meetings • New CDS onboarding • Quarterly Slide Training for CDS Onboarding will be shared between Supervisors with rotation based on new hire start date • Documentation Reviews and Suspecting Chart reviews for high priority / new providers / first WRVs / targeted lists • Attendance at targeted Clinical Documentation Reviews as needed • Partnership with Population Health Directors on general chart review support and strategies for region • Medical Records Access and review HIE/EMRs to identify potential suspects based on test results, imaging reports, etc. • Identify need for medical records requests from patient information, including payer data • Be an expert in tracking down and leveraging external resources, such as hospital records, Blue Button, and payer data, to support retrospective and prospective accurate documentation • Identify regional trends and training opportunities to support clinical documentation accuracy improvement • Identify and analyze opportunities for improving patient quality outcomes and cost of care • Analyze chronic condition prevalence based on patient demographics and identify opportunities for interventions • Structure initiatives to drive improvement in quality and risk adjustment documentation results • Monitor clinical documentation efforts • Develop predictive analytics insights • Other duties, as assigned