Role Description CentraCare is looking for a qualified Clinical Documentation Nurse to join our team! This role is responsible for concurrent auditing of medical record documentation to evaluate the documentation and utilization review of services to adequately reflect care provided and resources used. - Facilitation of appropriate physician documentation of care to accurately reflect patient severity of illness and risk of mortality. - Proactively solicits clarification from physicians and clinical staff in areas where further specificity is needed in the documentation. - Consults with attending physician when conflicting information appears in the medical record. - Maintains documentation regarding results of audit activity and shares those with staff and management as necessary. - Collects and analyzes data pertinent to documentation findings and outcomes for process improvement. - Supports the concepts and philosophies of nursing as well as sound business practices. - Promotes and facilitates education to providers regarding disease processes. - Communicates with appropriate healthcare team members to promote accurate and complete documentation of each patient encounter. Schedule: - Full-time | 80 hours every two weeks | Remote after training - Days | 8-hour shifts | Working hours between 6am-5pm - Occasional travel to CentraCare site required Pay and Benefits: - Starting pay begins at $87,193.60 per year; exact wage determined by years of related experience - Salary range: $87,193.60 - $130,873.60 per year - Salary and salary range are based on a 1.0 FTE, reduced FTE will result in a prorated offer rate - Full-time benefits: Medical, dental, PTO, retirement, employee discounts and more! - Tuition reimbursement and college grant programs available Qualifications - Bachelor's degree in nursing required - Current Registered Nurse (RN) licensure in the State of Minnesota required - Minimum of 3 years acute care experience required - Performance improvement, quality assurance related experience is required - Certified Clinical Documentation Specialist National Certification as Clinical Documentation Specialist (CCDS) preferred - National Certification as a Clinical Documentation Specialist-Outpatient (CCDS-O) preferred - Utilization review, coding, clinical informatics, case management or critical care experience preferred - Critical Thinking - must have the ability to process large amounts of information and to evaluate meaning with a rational open mind based on the evidence at hand. Company Description CentraCare has made a commitment to diversity in its workforce. All individuals including, but not limited to, individuals with disabilities, are encouraged to apply. CentraCare is an EEO/AA employer.

Role Description We are currently recruiting for a detail-oriented, team-focused Medical Writer with a focus in document quality control (QC). In this role, you will support Lexicon across multiple functional areas including: - Clinical Operations - Medical Affairs - Regulatory Affairs - External Affairs - CMC teams Your responsibilities will include: - Collaborating with functional areas to write, review, and QC documents including clinical study reports, protocols, Investigator Brochures, publications, presentations, and other clinical/regulatory documents for clarity, brevity, and consistency with the overall development program and source documents. - Driving the document development process for the functional review team, including using medical writing templates and document management software (e.g., StartingPoint and Veeva Vault). - Synthesizing clinical data, information, references, and other sources with input from SMEs program team members to prepare and present data and document messaging consistent with regulatory requirements, guidelines, and program strategy. - Reviewing and QCing documents. - Creating and managing document timelines. - Attending project-related meetings. - Assisting team members with document locations. - Developing and maintaining a Lexicon Style Guide. - Collaborating with vendors, which may include vendor oversight. - Identifying and appropriately communicating or escalating risks associated with document delivery or other writing-related issues. - Completing project-specific and company training, as assigned. Qualifications - Bachelor’s degree in healthcare or writing-related field required. - 5+ years technical or regulatory writing and/or QC experience; 2+ acceptable if in medical or regulatory writing. - Excellent QC skills. - Excellent writing and editing skills. - Excellent attention to detail—style, consistency, grammar, syntax, scientific accuracy. - Excellent interpersonal and oral communication skills. - Ability to communicate with professionals from a variety of backgrounds. - Strong knowledge of MS Word, Excel, PowerPoint, and Outlook. - Ability to prioritize multiple projects. - Project/time management and organizational skills, as well as the ability to work independently. - Flexibility in meeting challenging deadlines and changing requirements while working on multiple projects. - Comprehensive Microsoft Office skills, especially Word but also PowerPoint and Excel, as well as internet skills. - Knowledge of current requirements and guidelines applicable to submission documents. Company Description Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients’ lives. Through our unique approach to gene science based on Nobel Prize-winning technology, we are moving forward rapidly to bring innovative therapies to market. At Lexicon, our passion and dedication is driven by the patients for whom we work. Lexicon employees are inspired by the idea that their work can improve patients' lives and we know that our employees are essential to the success of our mission. Every day they bring their passion, talents and dedication to an engaging environment where they are rewarded with opportunities to realize their potential. We are dedicated to making Lexicon a great place to work by providing employees with the benefits, services, and programs as part of our total rewards package. For additional information about Lexicon and its programs, please visit www.lexpharma.com . Lexicon is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran. Lexicon Pharmaceuticals, Inc. is a drug-free workplace. Candidates are required to pass a drug test, background check, driving check (if applicable) and verification of credentials before beginning employment.

• writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences • demonstrates a command of relevant therapeutic areas and expertise with assigned products • analyzes, interprets, and applies clinical data to produce high-quality scientific communications • follows all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices

• Manage and facilitate anonymization of datasets and documents against planned timelines, in accordance with Incyte SOPs and regulatory requirements. • Assess documents in-scope for public disclosure according to EMA Policy 0070 and Health Canada PRCI. • Work closely with Biostatistics and Programing groups and Medical Writing teams to identify and assimilate the required documents and datasets. • Develop anonymization plans based on direct and indirect identifiers by measuring and mitigating re-identification risk according to GDPR guidance. • Process datasets and documents and apply required transformations. • Contribute to Anonymization Reports to support anonymization packages for policies of Health Canada and EMA. • Ensure accurate and consistent redaction of clinical trial documents to support EU CTR, ClinicalTrials.gov, and Publications. • Quality check of documents redacted/anonymized by other team members. • Collaborate with Regulatory Operations to ensure the publishing of redacted documents in the Regulatory Document Management System. • Experience with the use of Technology Tools for delivery of Anonymized Clinical Documents. • Assist in the development of internal work instructions, training materials, and procedures as needed to comply with global requirements and Incyte policies. • Ability to work with minimum supervision and resolve issues. • Develop and maintain collaborative relationships internally to ensure effective and efficient working relationships and the delivery of high quality deliverables. • Stay informed of new clinical trial disclosure and transparency requirements globally, including but not limited to clinical trial registration and posting of results.