Title: Regional Clinical Assessor (Hybrid Remote - (Sioux City, IA) Location: Sioux City United States Working time: Full-time Job Description: Description & Requirements Maximus is seeking a detail-oriented and compassionate Regional Clinical Assessor to join our team. In this role, you will conduct person-centered assessments for individuals seeking placement on Iowa Waivers or reassessment for those currently receiving waiver services, ensuring all activities align with state directives, MAXIMUS processes, and regulatory timeframes. This position offers the opportunity to make a meaningful impact by helping individuals access vital Medicaid Waiver and Long-Term Services and Supports. This is a hybrid role that includes frequent travel within the assigned areas of Iowa. Position is contingent upon contract award. Clinical licensure is not required for this role. About the Program: The IA CSA (Iowa Core Standardize Assessments) will conduct clinical assessments for individuals seeking enrollment into all Iowa Medicaid Waivers or to conduct clinical reassessments for Medicaid Waiver Recipients. Why Maximus? - Work/Life Balance Support - Flexibility tailored to your needs! - Competitive Compensation - Bonuses based on performance included! - ️ Comprehensive Insurance Coverage - Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance. - Future Planning - Prepare for retirement with our 401K Retirement Savings plan and Company Matching. - ️ Paid Time Off Package - Enjoy PTO, Holidays, and extended sick leave, along with Short and Long Term Disability coverage. - Holistic Wellness Support - Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP). - Recognition Platform - Acknowledge and appreciate outstanding employee contributions. - Tuition Reimbursement - Invest in your ongoing education and development. - Employee Perks and Discounts - Additional benefits and discounts exclusively for employees. - Maximus Wellness Program and Resources - Access a range of wellness programs and resources tailored to your needs. - Professional Development Opportunities-Participate in training programs, workshops, and conferences. - Licensures and Certifications-Maximus assumes the expenses associated with renewing licenses and certifications for its employees. Essential Duties and Responsibilities: - Responsible for completing medical and/or behavioral health assessments within contract requirements. - Conducts on-site, video call and/or telephonic assessments to determine an individual's needs for services and supports, eligibility, level of care or related outcome. - Perform all job duties in compliance with Person First standards, HIPAA guidelines, and company confidentiality policies and procedures. - Travel may be required based on program contract requirements. - Performs other related duties as assigned. - Preferred knowledge may include community support programs, long-term care assessment and level of care in medical, behavioral health or related programs. - Knowledge and understanding of medical and/or behavioral health diagnoses and prescribed medications. - Ability to collect data, define problems, establish facts, and draw valid conclusions. Minimum Requirements - Education and licensure requirements are based on program contract requirements and are outlined in job posting. - High School Degree or equivalent required. - Minimum 2 years of clinical experience required. - Bachelor's degree in health, social work, or a related field, or a master's degree in any field. - Minimum of two (2) years of experience in the human services field. - Familiarity with behavioral health diagnoses, psychotropic medications, and medical diagnoses. - Knowledge of diverse cultures with the ability to incorporate special needs into decision making. - Ability to work independently and collaboratively within a team. - Strong multitasking skills with the ability to prioritize and manage a high volume of tasks. - Strong written and verbal communication skills. - Proficiency in Microsoft Office Suite (Word, Outlook, Excel) and comfort working with various digital tools. - Ability to work effectively in a fast paced environment. - Professional interaction with external stakeholders (providers, physicians, state partners, etc.) Preferred Requirements - Prior experience using the InterRAI assessment system. - Experience working with Medicaid Waiver, Long Term Services and Supports, or similar programs. - Knowledge of state specific Medicaid Waiver regulations. - Familiarity with Person First standards and HIPAA compliance. - Additional certifications related to social work, healthcare, or human services are a plus. Home Office Requirements - Maximus provides company-issued computer equipment - Reliable high-speed internet service - Minimum 20 Mpbs download speeds/50 Mpbs for shared internet connectivity - Minimum 5 Mpbs upload speeds - Private and secure workspace #ClinicalServices EEO Statement Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. Pay Transparency Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances.

Title: Clinical Research Coordinators (Non-R.N.) Location: Salt Lake City United States Job Description: Bookmark this Posting Print Preview | Apply for this Job Announcement Details Requisition Number PRN44669B Job Title Clinical Research Coordinators (Non-R.N.) Working Title Clinical Research Coordinators (Non-R.N.) Career Progression Track P00 Track Level P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary Monday - Friday, 8:00 a.m. - 4:30 p.m. Hours may vary based on operational needs. Opportunities for a hybrid telework schedule may be considered after the initial training period, provided the arrangement is supported by operational needs and individual performance. Telework arrangements are not guaranteed and may be modified or discontinued at any time based on business requirements or performance. Employees approved for hybrid telework must provide their own private workspace, secure internet connection, and demonstrate the ability to work independently. VP Area U of U Health - Academics Department 00848 - Pediatric Administration Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range $38,500 - $52,314 (Note - Posting may close at any time) Job Summary Job Summary: The Department of Pediatrics, Division of Medical Genetics at the University of Utah School of Medicine has an immediate opening for a Clinical Research Coordinator. The Clinical Research Coordinator will coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations. Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care. Create and maintain tools and documentation to track study metrics, providing updates to management. Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities. Maintain source documents and report adverse events. Recruit, screen, enroll, and obtain consent from study participants. Collect and maintain patient and laboratory data. Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies. Work under the direction of the Primary Investigator (PI). Department Summary: The Department of Pediatrics is the second largest department in the University of Utah School of Medicine and one of the largest pediatric departments in the country. We are committed to improving the lives of children through excellence in advocacy, education, research, and clinical care. For more information about the Department of Pediatrics, please visit: http://medicine.utah.edu/pediatrics/. Mutual respect and appreciation are highly valued in the department. Benefits Summary: The University of Utah offers a comprehensive benefits package including: - Excellent health care coverage at affordable rates (see the Summary Comparison for more information) - 14.2% retirement contributions - Generous paid leave time - 11 paid Holidays per year - 50% tuition reduction for employees, spouses, and dependent children - Flex spending accounts - University provided basic employee life insurance coverage equal to a salary of up to $25,000 - Variety of elective insurance coverage, including life insurance, short and long-term disability, accidental death & dismemberment, accident, critical illness, hospital indemnity, and pet. - Free transit on most UTA services - Employee discounts on a variety of products and services, including cell phones & plans, entertainment, health and fitness, restaurants, retail, and travel - Professional development opportunities Additional benefits information is available at https://benefits.utah.edu/. Employee Health Requirements: This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations. Responsibilities Essential Functions: Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations. Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care. Create and maintain tools and documentation to track study metrics, providing updates to management. Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities. Maintain source documents and report adverse events. Recruit, screen, enroll, and obtain consent from study participants. Collect and maintain patient and laboratory data. Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies. Work under the direction of the Primary Investigator (PI). - Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and sponsor. - Attends and participates in Investigator and staff meetings. Advises team regarding specific study assignments and timelines. - Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety. - Determines length of visits and coordinates related facility and equipment availability. - Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. - Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. - Completes, audits, corrects CRFs, relays CRFs to sponsor. - Maintains documents as required by FDA guidelines. - Ensures proper collection, processing and shipment of specimens. Clinical Research Coordinator (Non-R.N.), I Requires basic skill set and proficiency. Conduct work assignments as directed. Closely supervised with little latitude for independent judgment. Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree. This is an Entry-Level position in the General Professional track. Job Code: PZ6511 Grade: P11 Expected Pay Range: $38,500 to $52,314 Disclaimer: This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job. Minimum Qualifications EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience). Department may hire employee at one of the following job levels: Clinical Research Coordinator (Non-R.N.), I: Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree. Preferences Preferences: - Prior clinical research experience preferred. Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; attention to detail; and the ability to function independently. Excellent interpersonal and communications skills, both oral and written. Proficiency in Microsoft Office and ability to learn new software programs. The Department will screen applicants according to the identified preferences. Type Benefited Staff Special Instructions Summary Additional Information The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at (801) 581-7447 for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions. Please contact Utah Retirement Systems at (801) 366-7770 or (800) 695-4877 or University Human Resource Management at (801) 581-7447 if you have questions regarding the post-retirement rules. This position may require the successful completion of a criminal background check and/or drug screen. The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education. Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both. To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX (OEO). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at the: University of Utah Non‑Discrimination page. https://publicsafety.utah.edu/safetyreport/ This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South. As per University of Utah policy 5-108: Transfer of Benefits Eligible Staff Members, a new hire to the University of Utah who is still serving a 12 month probationary period will not be hired into another University of Utah job (a transfer) until the successful completion of the probationary period. Posting Specific Questions Required fields are indicated with an asterisk (*). - - What is your highest level of completed education? - None - High School Diploma or Equivalent - Associate Degree - Bachelor's Degree - Master's Degree - Doctorate Degree - - How many years of related work experience do you have? - Less than 2 years - 2 years or more, but less than 4 years - 4 years or more, but less than 6 years - 6 years or more, but less than 8 years - 8 years or more, but less than 10 years - 10 years or more, but less than 12 years - 12 years or more, but less than 14 years - 14 years or more - - Do you have a working knowledge of Good Clinical Practices, FDA, HIPAA, and IRB regulations? - Have knowledge in all of these areas - Have knowledge in some of these areas, but not all - No previous knowledge in these areas - - Please indicate your skill level in the Microsoft Office suite - None - Minimal - Moderate - Extensive

Coordinate and evaluate clinical trial conduct, ensure adherence to protocols, maintain accurate documentation, and provide patient education and support throughout the research process while advocating for participants and families.

• Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements • Screen and evaluate potential research participants for eligibility, documenting inclusion/exclusion criteria and escalating complex questions as needed • Manage scheduling and execution of virtual and home-based study visits, assessments, and follow-up activities • Collect, review, and enter study data accurately and in a timely manner using EDC systems and study tools • Maintain complete, accurate, and audit-ready study documentation, including regulatory binders, participant records, and tracking logs • Conduct or support informed consent discussions in both Spanish and English, ensuring proper documentation and compliance • Serve as a primary point of contact for research participants and caregivers, including Spanish-speaking populations • Prepare for and support sponsor, IRB, and regulatory monitoring visits, including responding to document requests and resolving findings • Track and report study metrics such as enrollment, retention, deviations, and visit completion • Identify operational risks or inefficiencies and proactively communicate improvement opportunities to research leadership • Collaborate closely with investigators, care coordinators, and cross-functional teams to ensure a high-quality research experience • Support onboarding and informal mentoring of junior research staff, as appropriate