NewEntry Level Regulatory Affairs Specialist HarveStaffEntry Level Regulatory Affairs SpecialistChesterfield, MO$32.30–$40.30 / hourbody { font-family:'Times New Roman'; font-size:12pt } h1, h2, h3, p { margin:0pt } li { margin-top:0pt; margin-bottom:0pt } h1 { margin-top:12pt; page-break-inside:avoid; page-break-after:avoid; font-family:'Helvetica Neue'; font-size:16pt; font-weight:normal; color:#0079bf } h2 { margin-top:2pt; page-break-inside:avoid; page-break-after:avoid; font-family:'Helvetica Neue'; font-size:13pt; font-weight:normal; color:#0079bf } h3 { margin-top:2pt; page-break-inside:avoid; page-break-after:avoid; font-family:'Helvetica Neue'; font-size:12pt; font-weight:normal; color:#00507f }. This role manages regulatory documentation, maintains tracking systems, and coordinates with regulatory agencies to support timely product registrations.
NewRegulatory Affairs Specialist (Entry) TekWissen LLCRegulatory Affairs Specialist (Entry)Chesterfield, MORemote$34.50This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world, headquartered in Leverkusen, and areas of business include pharmaceuticals; consumer healthcare products, agricultural chemicals, seeds and biotechnology products. Tasks and Responsibilities: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA Sections 3, 24(c), 2(ee), 18, 5 for crop protection products.
Senior CMC Regulatory Affairs Scientist Actalent IncSenior CMC Regulatory Affairs ScientistBridgeton, MORemote$53–$72.12 / hourThe position serves as a technical-regulatory expert, partnering closely with R&D, pharmaceutical development, industrial operations, and external partners to optimize regulatory strategies, streamline data use globally, and support both pre- and post-approval activities. The Senior CMC Regulatory Affairs Scientist leads the design and evaluation of chemistry, manufacturing, and controls (CMC) studies to meet regulatory requirements and defines robust regulatory strategies for United States submissions.
New**Senior CMC Regulatory Affairs Scientist** Actalent Inc**Senior CMC Regulatory Affairs Scientist**Bridgeton, MORemote$53–$72.12 / hourThe position serves as a technical-regulatory expert, partnering closely with R&D, pharmaceutical development, industrial operations, and external partners to optimize regulatory strategies, streamline data use globally, and support both pre- and post-approval activities. The Senior CMC Regulatory Affairs Scientist leads the design and evaluation of chemistry, manufacturing, and controls (CMC) studies to meet regulatory requirements and defines robust regulatory strategies for United States submissions.
NewRegulatory Affairs Specialist -32983 The Kemtah Group, Inc.Regulatory Affairs Specialist -32983Chesterfield, MORemoteRemote Position TASKS AND RESPONSIBILITIES: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products Communicate with State regulatory agencies regarding submissions, approvals, renewals Maintain and update regulatory databases and other internal tracking systems. Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience Proficiency in the Microsoft Office suite Database Management experience Experience with document comparison tools is a plus.
NewRegulatory Affairs Specialist -32982- hybrid The Kemtah Group, Inc.Regulatory Affairs Specialist -32982- hybridChesterfield, MOHybrid position TASKS AND RESPONSIBILITIES: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products Communicate with State regulatory agencies regarding submissions, approvals, renewals Maintain and update regulatory databases and other internal tracking systems. Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience Proficiency in the Microsoft Office suite Database Management experience Experience with document comparison tools is a plus.
NewRegulatory Affairs Specialist - Agriculture Remote BelcanRegulatory Affairs Specialist - Agriculture RemoteChesterfield, MORemoteRemote Position TASKS AND RESPONSIBILITIES: * Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products * Communicate with State regulatory agencies regarding submissions, approvals, renewals * Maintain and update regulatory databases and other internal tracking systems. * Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: * BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience * Proficiency in the Microsoft Office suite * Database Management experience * Experience with document comparison tools is a plus.
NewRegulatory Affairs Specialist - Agriculture Hybrid BelcanRegulatory Affairs Specialist - Agriculture HybridChesterfield, MOHybrid position TASKS AND RESPONSIBILITIES: * Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products * Communicate with State regulatory agencies regarding submissions, approvals, renewals * Maintain and update regulatory databases and other internal tracking systems. * Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: * BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience * Proficiency in the Microsoft Office suite * Database Management experience * Experience with document comparison tools is a plus.
Analyst II, Rates and Regulatory Affairs Liberty Utilities (Canada) Corp.Analyst II, Rates and Regulatory AffairsMO$75,000–$100,000 / yearThe Regulatory Analyst will report to the Director, Rates and Regulatory Affairs, and will undertake complex financial and operational research and analysis for priority regulatory projects or rate issues for Liberty's Central Region Utilities. Our rapid growth has led both our regulated utility services and renewable energy business groups into different geographies and commodities, but our purpose remains unchanged - Sustaining Energy and Water for Life.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaMO$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
NewRegulatory Affairs Specialist - Agriculture Hybrid Belcan LLCRegulatory Affairs Specialist - Agriculture HybridChesterfield, MOTASKS AND RESPONSIBILITIES: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products. Track and Process payment of state registration fees, including new product registration fees, annual state renewal fees.
NewRegulatory Affairs Specialist - Agriculture Remote Belcan LLCRegulatory Affairs Specialist - Agriculture RemoteChesterfield, MORemoteTASKS AND RESPONSIBILITIES: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products. Track and Process payment of state registration fees, including new product registration fees, annual state renewal fees.
NewRegulatory Affairs Specialist (Entry) # 26-17692 US Tech Solutions, Inc.Regulatory Affairs Specialist (Entry) # 26-17692Chesterfield, MO$35–$40 / hourResponsibilities: Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA Sections 3, 24(c), 2(ee), 18, 5 for crop protection products. Track and Process payment of state registration fees, including but not limited to, new product registration fees, annual state renewal fees, tonnage etc.
Senior Regulatory Affairs Specialist - Global Pet Care Spectrum Brands Holdings IncSenior Regulatory Affairs Specialist - Global Pet CareSt. Louis, MOThe above information on this description has been designed to indicate the general nature and level of work performed by employees within this job/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 this job.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsJefferson City, MORemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
Executive Director Business Affairs - Neurology Washington University in St LouisExecutive Director Business Affairs - NeurologySt. Louis, MOSkills: Budget Preparation, Business Information Systems, Business Planning, Effective Written Communication, Financial Analysis, Financial Forecasting, Financial Institution Management, Financial Systems, Group Presentations, Interpersonal Communication, Medical Office Administration, Oral Communications, Teamwork. The department's research spans basic, translational, and clinical investigation, supported by extensive laboratory and research center infrastructure, including the Hope Center for Neurological Disorders and the Knight Alzheimer Disease Research Center, and is characterized by strong cross-disciplinary collaboration across WashU Medicine.
Vice President, State Governmental Affairs RGAVice President, State Governmental AffairsMissouriRemoteThe Vice President, State Governmental Affairs is responsible for developing and leading RGA's state‑level government relations strategy across the United States, including at the National Association of Insurance Commissioners (NAIC). This role provides enterprise leadership on legislative and regulatory engagement within a highly regulated environment, with a focus on protecting RGA's business interests, managing regulatory risk, and supporting long‑term growth.
Manager, External Affairs Liberty Utilities (Canada) Corp.Manager, External AffairsJoplin, MOProvides additional support to the Senior Director of Regulatory and Government Affairs on Missouri legislative, regulatory and stakeholder matters; and to the Senior Manager of Community Affairs and Strategic Accounts on municipal and community stakeholder engagement in the Joplin area. Supports Liberty's electric utility business in the Central region-Arkansas, Kansas, Missouri, and Oklahoma-through strategic engagement with government officials, regulators, and industry stakeholders across the service territory.
Vice President, State Governmental Affairs Reinsurance Group of America IncVice President, State Governmental AffairsSt. Louis, MORemote$150,770–$224,640 / yearThe Vice President, State Governmental Affairs is responsible for developing and leading RGA's state‑level government relations strategy across the United States, including at the National Association of Insurance Commissioners (NAIC). This role provides enterprise leadership on legislative and regulatory engagement within a highly regulated environment, with a focus on protecting RGA's business interests, managing regulatory risk, and supporting long‑term growth.
NewOffice of Compliance and Legal Affairs - Student Employee Maryville UniversityOffice of Compliance and Legal Affairs - Student EmployeeSt. Louis, MOSpecial Projects: Assist with the implementation of new regulations and coordinate special initiatives, such as organizing Compliance and Ethics Week and preparing the annual licensure compliance report and launching the office's SharePoint site. The position offers hands-on experience in compliance, risk management, and legal operations within a higher education setting, with exposure to policy research, compliance monitoring, training development, and administrative support.
Community Affairs & Strategic Accounts Manager II Liberty Utilities (Canada) Corp.Community Affairs & Strategic Accounts Manager IIMOThe Manager, Strategic Growth & Community Affairs leads the company's engagement with strategic and high-value accounts, including major commercial, industrial, municipal customers and local elected officials. Lead the management of the company's largest and most strategic customer accounts, building trusted relationships, identifying growth opportunities, and ensuring exceptional customer service and retention.
NewSenior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO) University of Kansas Medical CenterSenior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)Kansas City, MO$60,800–$91,200 / yearJob Description Summary: The Senior Regulatory Coordinator within the Comprehensive Integrated Research Operations (CIRO) department serves as the administrative resource and liaison involved in supporting the business aspects of the clinical research enterprise. The Senior Regulatory Coordinator is responsible for leading and performing study-specific regulatory and safety reporting for a group of investigators, within multiple cost centers in the Department of Internal Medicine.
NewSenior Regulatory Accounting Analyst NACBASenior Regulatory Accounting AnalystKansas City, MOSummit Utilities Join our Growing Team and see why Summit Utilities, Inc was named as one of the Fastest Growing Denver Area Private Companies 2019 and 2020; Best Places to Work in Maine 2019, 2020, 2021, 2022 and 2023; and Best Places to Work in Arkansas 2020 and 2023, Oklahoma 2022 and 2023 and Missouri 2023. Knowledge, Skills, AbilitiesKnowledgeable and experienced in the administrative aspects of management in a corporation including assisting in setting and communicating goals, delegating, providing feedback to employees, handling employee issues, and providing employee recognition.
Research Compliance Officer - Partnerships, Office of Research and Innovation University of MissouriResearch Compliance Officer - Partnerships, Office of Research and InnovationKansas City, MO$69,097.60–$80,000 / year3-5 years of experience in research administration, compliance, Institutional Review Board and Institutional Animal Care and Use Committee support, regulatory affairs, human subjects research (via Institutional Review Board), animal research compliance (via Institutional Animal Care and Use Committee), and /or research integrity, regulatory compliance, or audit functions is strongly preferred. Independent Regulatory Review & Determination: Perform comprehensive, substantive reviews of research protocols (specifically Exempt and Expedited categories) to evaluate ethical design and regulatory adherence; independently issue determinations, request stipulations, and approve protocols in accordance with federal regulations (Common Rule, FDA) and UMKC policy.
Quality Manager (40382) Young Innovations IncQuality Manager (40382)MO$110,000–$140,000 / yearInitiate and implement quality improvement activities as appropriate to raise the quality and compliance of the site's product line and processes, which includes educating and training employees on the Quality Management System. Establish and implement metrics (process capability, control charts, measurement quality) for monitoring system effectiveness and to enable managers to make sound product quality decisions.
Sr. Compliance Specialist Thermo Fisher Scientific IncSr. Compliance SpecialistSt. Louis, MOREQUIREMENTS: Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in compliance, quality systems, or regulatory affairs. The Senior Regulatory Compliance Specialist is responsible for leading and managing regulatory compliance activities with a strong focus on health authority and client audits.
EPR & Product Stewardship Specialist BPS Direct LLCEPR & Product Stewardship SpecialistSpringfield, MOThe position requires hands-on management of regulatory filings, data collection, consultant oversight, and cross-functional coordination to maintain compliance and audit readiness across packaging, electronics/batteries, vehicle/boat components, bottle bills, plastics/PFAS, recycling labeling, and other emerging product stewardship programs. Execute or coordinate execution of EPR registrations, reporting, and filings across U.S. state packaging EPR programs and Canadian provincial programs; maintain or coordinate maintenance of Producer Responsibility Organization (PRO) relationships.
Director of Compliance Swope HealthDirector of ComplianceKansas City, MissouriThe Director develops and implements the corporate compliance program, oversees risk mitigation strategies, and ensures organizational policies and procedures promote ethical conduct, regulatory compliance, and quality improvement. Since then, Swope has since expanded its size, scope, and service offerings to include behavioral and dental care, services for the unhoused, mobile services and school-based clinics, and the PACE KC Adult Wellness Center.
Compliance Coordinator Stride, Inc.Compliance CoordinatorJefferson City, MissouriPrimary responsibilities include but are not limited to the submission of new and renewal applications, student performance data to various oversight agencies, maintaining point of contact information for oversight agencies, processing employment verifications, and distribution of internal compliance updates. The company partners with workforce organizations, healthcare providers, and academic institutions to help build talent pipelines and provide pathways to career advancement, including opportunities for articulated college credit.
Director of Compliance Swope Health ServicesDirector of ComplianceKansas City, MOPart timeThe Director develops and implements the corporate compliance program, oversees risk mitigation strategies, and ensures organizational policies and procedures promote ethical conduct, regulatory compliance, and quality improvement. Since then, Swope has since expanded its size, scope, and service offerings to include behavioral and dental care, services for the unhoused, mobile services and school-based clinics, and the PACE KC Adult Wellness Center.
Life Sciences Supply Chain and Operations - Supply Chain Planning Manager Accenture PlcLife Sciences Supply Chain and Operations - Supply Chain Planning ManagerSt. Louis, MOAs part of working with clients you will help with several aspects of life sciences integrated planning including: Integrated Planning Strategy: Design and implement IBP/S&OP frameworks tailored to life sciences environments, accounting for regulatory release cycles, CMO/CDMO network complexity, and the distinct planning dynamics of biopharma and med tech product portfolios. Accenture is a leading solutions and services company that helps the world's leading enterprises reinvent by building their digital core and unleashing the power of AI to create value at speed across the enterprise, bringing together the talent of our approximately 786,000 people, our proprietary assets and platforms, and deep ecosystem relationships.
Director, Quality Assurance - Medical Device Services (Multi-Site) Eurofins Scientific SEDirector, Quality Assurance - Medical Device Services (Multi-Site)Maryland Heights, MOIn addition to leading Quality for Medical Device Services, the Senior Director will serve as an active member of the North America Quality Leadership Team, collaborating with Quality leaders across the BioPharma Product Testing (BPT) and Medical Device Services (MDS) businesses to advance enterprise-wide Quality initiatives, share best practices, harmonize Quality systems where appropriate, and strengthen a consistent culture of Quality across laboratories and business segments while recognizing the unique regulatory requirements of each market. The successful candidate will lead the transformation and harmonization of Quality Management Systems across a growing network of laboratories and consulting businesses while supporting acquisitions, new service offerings, laboratory expansions, and future growth into medical device product development and engineering services.
NewVice President Internal Audit and Compliance Wisconsin Physicians Service Insurance CorpVice President Internal Audit and ComplianceKansas City, MORemote$235,000–$275,000 / yearThis Vice President drives continuous improvement, fosters a culture of integrity, and represents the Audit and Compliance functions in high visibility forums, including presentations to executive leadership and the Audit, Compliance & Risk Committee of the Board. We are open to remote work in the following approved states: Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, Nebraska, New Jersey, North Carolina, Ohio, South Carolina, Texas, Virginia, Wisconsin.
Associate Director, Health IT Taylor Strategy PartnersAssociate Director, Health ITSaint Louis, MORemote$140,000–$180,000 / yearArrowhead Pharmaceuticals is seeking an Associate Director to focus on identifying unmet needs and gaps in care across health systems for patients with rare cardiovascular diseases. This role emphasizes understanding how health information technologies and real-world evidence can help close care gaps, improve patient identification, and drive better outcomes.
Medical Science Liaison: Med Device - Interventional Oncology Becton Dickinson and CoMedical Science Liaison: Med Device - Interventional OncologySt Louis, MO$159,800–$255,700 / yearAssist in facilitating KOL (Key Opinion Leader) involvement in national, regional, and local educational forums including advisory boards, investigator meetings, educational symposia, and sponsored promotional programs. Establish and maintain credible peer-to-peer scientific relationships with national/regional key opinion leaders (KOLs) Healthcare professionals (HCPs), and other stakeholders in the interventional oncology field.
Import Processing Representative I Ascent Global Logistics Holdings IncImport Processing Representative ISpringfield, MOInvolves a high degree of responsibility for working with, safeguarding and controlling highly restricted information, knowledge or important confidences and criterion-related to research and development of customer data, future plans, policies, business prospects, finances, etc. the release of which could have a detrimental effect and impact on the company's affairs or undermine its competitive position. The company connects customers to its extensive carrier network, internal ground fleet and airline via its proprietary, digital PEAK freight marketplace, which provides robust carrier capacity and transparent pricing, backed by 24/7/365 logistics experts.
Budget Analyst - Comprehensive Integrated Research Operations University of Kansas Medical CenterBudget Analyst - Comprehensive Integrated Research OperationsKansas City, MO$60,800–$91,200 / yearSupport grant opportunities, facilitate proposal development, contribute to non-technical components of proposals, process proposals, develop budgets, support contract development, and ensure compliance with laws, regulations, policies, and terms and conditions. Job Description: Job Duties: • Manage and perform activities related to multiple areas of sponsored projects administration, including but not limited to pre-award and post-award activities for multiple cost centers.
Executive Director, Center for Advanced Dental Education Saint Louis UniversityExecutive Director, Center for Advanced Dental EducationMOSLU School of Medicine is grounded in an understanding of the scientific method and an appreciation for personal commitment and service to others, and these diverse educational experiences prepare individuals for careers and leadership roles in medicine and the medical sciences. The Executive Director oversees the education of residents in one of four specialties: endodontics (6 residents; 24-months), orthodontics (42 residents; 30-months), pediatric dentistry (6 residents; 24-months), or periodontics (9 residents; 36-months).
SYSTEM ENGINEER ApolisSYSTEM ENGINEERHazelwood, MO$1 / hourThe role also acts as an Onsite Coordinator, bridging communication between offshore teams and customer stakeholders. Onsite Coordinator Responsibilities Primary interface between customer (onsite) and offshore delivery teams.
Operations Manager 51 Elementis Specialties USAOperations ManagerSaint Louis, MissouriCombining our leading positions in the science of materials flow, surface modification, and formulation with access to unique natural materials, Elementis delivers unique chemistry, sustainable solutions to customers in a wide range of markets, including cosmetics, anti-perspirants, decorative and industrial coatings, automotive and ceramics. Higher-level approvals are required for decisions involving significant capital investments, major process redesigns, adoption of new technologies with long-term implications, or strategic engineering changes that impact regulatory compliance or overall business direction.
Technical Specialist - KRYPTOR Systems and Assays Thermo Fisher Scientific IncTechnical Specialist - KRYPTOR Systems and AssaysMODiscover Impactful Work: As a Technical Specialist - KRYPTOR Systems and Assays, you will play a critical role in supporting customers and internal partners with deep technical and laboratory expertise related to the KRYPTOR compact plus, KRYPTOR gold, and associated assays. This field-facing technical specialist role serves as a key laboratory and scientific resource for internal teams and external customers combining scientific education, technical consultation, assay implementation, validation support, troubleshooting, and customer enablement activities across both clinical and research environments.
Director, Research Lindenwood UniversityDirector, ResearchSt. Charles, MOWorking collaboratively with University leadership, faculty, staff, students, and external partners, the Director advances research, scholarship, creative activity, sponsored projects, and research compliance by providing leadership for research administration, grant development and management, human subjects research, internal funding programs, research ethics, and faculty and student research support. Provides university-wide leadership for the Office of Research, Compliance, and Academic Affairs (ORCA), including research administration, research development, sponsored projects, internal funding, human subjects research compliance, research ethics, data management, intellectual property support, and faculty/student research consultation.
Senior Director, MSAT Thermo Fisher Scientific IncSenior Director, MSATSt. Louis, MOThe Senior Director serves as a trusted executive partner to global biotechnology and pharmaceutical clients, building long-term strategic relationships and providing scientific leadership through governance forums, Joint Steering Committees, regulatory interactions, and commercialization planning. How will you make an impact: The Senior Director, Manufacturing Sciences and Technology (MSAT), serves as the strategic and scientific leader for all technology transfer, process validation, continued process verification, product lifecycle management, and manufacturing process support activities for the St.
Associate General Counsel (MedInsight) Milliman IncAssociate General Counsel (MedInsight)St. Louis, MORemote$181,400–$354,660 / yearMedInsight is a subsidiary of Milliman; a global, employee-owned consultancy providing actuarial consulting, retirement funding and healthcare financing, enterprise risk management and regulatory compliance, data analytics and business transformation as well as a range of other consulting and technology solutions. We are looking for a candidate with proven experience at the intersection of healthcare and technology, with specialized knowledge in healthcare data privacy, clinical data acquisition and interoperability, consumer and data protection, AI and emerging technology governance, and data licensing and commercialization agreements.
Advanced Medical Support Assistant U.S. Department of Veterans AffairsAdvanced Medical Support AssistantJefferson Barracks, MO$54,307–$70,599 / yearOther assignments at this level include, but are not limited to: processes incoming patient secure messaging through MyHealthyVet and coordinates with care team as appropriate; participates in team huddles and team meetings to manage, plan, problem solve, and follow-up with patient care by sharing information and collaborating with the interdisciplinary team; setting priorities and deadlines, adjusting the flow and sequencing of the work to meet team and patient needs; identifies incomplete encounters and communicates findings to providers; as needed; assists the team to reinforce the plan of care and self-help solutions; enters appropriate information into the electronic record; monitors pre-appointment information and/or requirements to assure readiness for patient visit/procedure; manages patient systems to verify and validate accuracy and resolve issues; evaluates patient information and clinic schedule lists to determine whether the patient requires an immediate appointment; informs team members about shared patients ([i.e]., those who receive their care at multiple VA centers or those who receive care in the community). MSAs at this level develop and/or maintain effective and efficient communication with the patient, interdisciplinary coordinated care delivery model teams, VA medical centers, and other agencies (e.g., assist with communications during the inpatient to outpatient discharge; communicate with non-VA medical facilities; prepare correspondence to notify patients of normal lab results; manage a system for follow-up care such as consults, tests, etc.).
Medical Support Assistant (Advanced) U.S. Department of Veterans AffairsMedical Support Assistant (Advanced)Columbia, MO$53,532–$69,591 / yearProvides complete appointment management according to clinic guidelines, to include scheduling, cancelling, and re-scheduling patient appointments and/or consults; enters no-show information; ensures encounters that need Action Required are completed in order to obtain appropriate workload credit; verifies and updates demographics and insurance information, among other aspects of appointment management. Advanced knowledge of policies and procedures associated with interdisciplinary coordinated care delivery and/or care in the community operational activities that affect patient flow, and patient support care administrative functions to include, but not limited to appointment cycles, outside patient referrals, follow-up care, overbooking, provider availability, etc.
Director of Policy Health Forward FoundationDirector of PolicyKansas City, Missouri$140,800–$176,000 / yearFull timeOur work includes supporting equitable health care access and outcomes; working to advance safe and affordable housing, pathways to home ownership and broadband access; amplifying the power that exists in our communities through civic engagement and supporting grassroots nonprofits; shifting narratives that impact our prioritized communities of focus. Health Forward is driven by the data evidencing health inequities and is committed to the process and the outcome of equity, inclusion, and anti-racism in our grant and gift funding, policy and advocacy, community engagement, employment practices, talent management, investments, vendor selection, and governance.
Social Worker - Residential Substance Use Disorder U.S. Department of Veterans AffairsSocial Worker - Residential Substance Use DisorderKansas City, MO$76,902–$120,965 / yearAt the time of appointment, the supervisor, chief social work or social work executive will provide the unlicensed/uncertified social worker with the written requirements for licensure or certification, including the time by which the license or certification must be obtained and the consequences for not becoming licensed or certified by the deadline. Duties include but are not limited to: The incumbent serves as a Clinical Social Worker within the Residential Substance Use Disorder (SUD) Treatment Program, providing advanced practice social work services to Veterans with substance use disorders and co-occurring mental health conditions.
Senior Clinical Research Coordinator - Pediatrics University of Kansas Medical CenterSenior Clinical Research Coordinator - PediatricsKansas City, MO$70,200–$105,300 / yearThe SCRC collaborates with investigators, sponsors, and research staff to facilitate study conduct, contributes to study budgets and regulatory submissions, participates in quality assurance activities, and provides guidance to Clinical Research Coordinators as needed. Job Description Summary: The Senior Clinical Research Coordinator (SCRC) in the Department of Pediatrics manages clinical research studies by overseeing complex activities related to the collection, documentation, and analysis of research data in accordance with regulatory requirements and institutional policies.
Senior MSL - Mid WestMultiple Territories Definium Therapeutics IncSenior MSL - Mid WestMultiple TerritoriesMO$225,560–$255,000 / yearOur lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Additionally, this role will also help shape internal resources, training, and capabilities for the broader Field Medical Function The ideal candidate will have a deep understanding of psychiatric disorders, a passion for science-driven conversations, and the ability to operate effectively in a small, fast-growing biotech environment.