Compliance Analyst – Complaints & Regulatory Affairs Advisors ExcelCompliance Analyst – Complaints & Regulatory AffairsLenexa, KansasPosition: Compliance Analyst - Complaints & Regulatory Affairs Department: Compliance Reporting to: Compliance Director Location: Lenexa, KS/ Topeka, KS - Onsite Overview: The Compliance Analyst plays a key role in maintaining Advisors Excel's regulatory standing by investigating/reviewing complaints, supporting regulatory exam readiness, and assisting with regulatory inquiries alongside the Compliance Director and Regulatory Counsel. What you’ll do: Investigate complaints thoroughly - When a complaint comes in, you'll dig into what happened, gather the relevant documents and details, and work through the facts carefully to reach a fair and well-supported resolution.
Compliance Analyst - Complaints & Regulatory Affairs Advisors Excel LLCCompliance Analyst - Complaints & Regulatory AffairsLenexa, KSOverview: The Compliance Analyst plays a key role in maintaining Advisors Excel''s regulatory standing by investigating/reviewing complaints, supporting regulatory exam readiness, and assisting with regulatory inquiries alongside the Compliance Director and Regulatory Counsel. What you'll do: Investigate complaints thoroughly - When a complaint comes in, you''ll dig into what happened, gather the relevant documents and details, and work through the facts carefully to reach a fair and well-supported resolution.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaKS$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.
Senior Regulatory Affairs Manager Argenta LtdSenior Regulatory Affairs ManagerShawnee, KSRemoteRequirements: Bachelor's degree or equivalent experience in a scientific discipline, advanced degree (DVM, PhD, MS) is preferred 8+ years experience in veterinary regulatory and/or animal drug development Proven experience includes several of the following: CVM, E-Submitter, GLP, GCP, GMP, USDA, EPA, EMA Development and regulatory experience with food animal drugs is preferred but not required Good written and oral communication skills, and ability to work collaboratively within and across teams Results and bottom line oriented Excellent analytical skills and attention to detail Proven influence, negotiation and persuasion skills Defines and plans priorities well. About the role: Facilitates and supports the regulatory and drug development requirements of external clients and internal projects Effectively manage client and stakeholder expectations by providing timely, relevant, and accurate documents, assessments, reports and communications Demonstrates an awareness of current regulations, guidances, regulatory processes, and the animal drug development process, while maintaining a flexible and creative mindset to work through regulatory challenges Creates regulatory solutions to complex issues Provides client accurate expert regulatory advice on animal health product development Represent Argenta in industry associations (e.g.
Sr Director, Sci Affairs & Innovation Colgate-Palmolive CoSr Director, Sci Affairs & InnovationOverland Park, KS$245,000–$275,000 / yearThis role reports to the Global Chief Veterinary Officer and supports the execution of strategies that position Hill's as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill's product superiority, and demonstrating our commitment to transforming the lives of people and their pets. GPVA (Global Professional and Veterinary Affairs) plays an integral role in positioning Hill's in the global profession as a scientific, innovative and credible partner who is engaged in improving the health of dogs and cats, and in supporting the profession.
Sr Director, Sci Affairs & Innovation (Overland Park, KS, US) Colgate-Palmolive CompanySr Director, Sci Affairs & Innovation (Overland Park, KS, US)Overland Park, KS$245,000–$275,000 / yearThis role reports to the (Global) Chief Veterinary Officer and supports the execution of strategies that position Hill’s as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill’s product superiority, and demonstrating our commitment to transforming the lives of people and their pets. This role supports the execution of strategies that position Hill’s as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill’s product superiority, and demonstrating our commitment to transforming the lives of people and their pets.
Attorney - Manager of Legal Affairs QCHI/ LendNation Open CareerAttorney - Manager of Legal AffairsLenexa, KansasSuccess in this role will require strong legal research and analytical skills, sound judgment, the ability to evaluate statutory and regulatory requirements, often on tight timelines, and the ability to communicate practical, business-focused guidance to non-legal stakeholders in a clear and effective manner. The attorney in this role will help support the development, structure, and ongoing administration of financial products, while also advising business partners on legal and regulatory requirements that affect day-to-day operations and longer-term strategic initiatives.
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.
Manager of Legal Affairs QCHIManager of Legal AffairsLenexa, KSSuccess in this role will require strong legal research and analytical skills, sound judgment, the ability to evaluate statutory and regulatory requirements, often on tight timelines, and the ability to communicate practical, business-focused guidance to non-legal stakeholders in a clear and effective manner. The attorney in this role will help support the development, structure, and ongoing administration of financial products, while also advising business partners on legal and regulatory requirements that affect day-to-day operations and longer-term strategic initiatives.
NewRegulatory Compliance Manager Argenta LtdRegulatory Compliance ManagerShawnee, KSIn-depth knowledge of FDA regulations, EU GMP, and ICH guidelines Strong understanding of cGMP requirements across dosage forms Experience with state licensing Experience with DEA Proven experience in regulatory inspection management and client-facing compliance reporting Ability to interpret regulatory requirements and translate into practical site-level compliance actions. The Compliance Manager partners closely with cross-functional teamsincluding Quality Assurance, Operations, Regulatory Affairs, and Client Services to ensure robust systems are in place andfunctioning effectively.
Associate Director, Regulatory Compliance and Quality Systems Catalent IncAssociate Director, Regulatory Compliance and Quality SystemsKansas City, MOThe Associate Director, Regulatory Compliance and Quality Systems is responsible for the strategy and processes required to maintain a state of regulatory compliance at the KCM site through Audit Ready 365, Quality Technical Agreements, support of Client regulatory filings, state licensure, Commercial Data Reports while maintaining oversight of the Quality Systems programs including Supplier Management, Material Review Board, Internal Audits, Client Audits, Training, Document and Change Control, Record Management, Trackwise and other issues and actions as needed. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Associate Director, Regulatory Compliance and Quality Systems CatalentAssociate Director, Regulatory Compliance and Quality SystemsKansas City, MissouriThe Associate Director, Regulatory Compliance and Quality Systems is responsible for the strategy and processes required to maintain a state of regulatory compliance at the KCM site through Audit Ready 365, Quality Technical Agreements, support of Client regulatory filings, state licensure, Commercial Data Reports while maintaining oversight of the Quality Systems programs including Supplier Management, Material Review Board, Internal Audits, Client Audits, Training, Document and Change Control, Record Management, Trackwise and other issues and actions as needed. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Clinical Research Associate (CRA) - Oncology (Remote) Merck & Co IncClinical Research Associate (CRA) - Oncology (Remote)Kansas City, MORemote$96,200–$151,400 / yearConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
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.
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 ManagerOverland Park, KSAs 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 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.
Lab Coordinator, Chemistry JCCCLab Coordinator, ChemistryOverland Park, Kansasor Director of Human Resources, or the Dean of Students and Learner Engagement at Johnson County Community College, 12345 College Blvd, Overland Park, KS 66210, 913-469-8500; or to Office for Civil Rights, Kansas City Office, U.S. Department of Education, One Petticoat Lane, 1010 Walnut Street, Suite 320, Kansas City, MO 64106, Telephone: 816-268-0550, Facsimile: 816-268-0559, Email to: OCR.KansasCity@ed.gov. Assess and maintain safety equipment, including eye washes, safety showers, and spill kits, to ensure operability and suitability to activities performed in the lab in compliance with regulatory requirements and industry best practices.
Managed Services Sr. Consultant Deloitte Touche Tohmatsu LtdManaged Services Sr. ConsultantMO$120,200–$140,000 / yearLead and contribute to end-to-end delivery for Generis CARA and associated regulatory technology platforms - including requirements gathering, solution design, system configuration, content template development, and user acceptance testing. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
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.
Oncology Nurse Educator - Midwest and Central PharmaEssentia CorpOncology Nurse Educator - Midwest and CentralMO$157,080–$204,000 / yearFounded in 2003 by a team of Taiwanese-American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taiwan Stock Exchange (TWSE: 6446) and are expanding our global presence with operations in the U.S., Japan, Singapore, South Korea, and China, along with a world-class biologics production facility in Taichung. Position Overview: The Oncology Nurse Educator is responsible for delivering non-promotional, compliant clinical education to healthcare offices, nurses, nurse practitioners, physician assistants, and other clinical staff involved in the treatment of patients receiving BESREMi.
NewAssociate Director, Engineering Merck & Co IncAssociate Director, EngineeringDe Soto, KS$142,400–$224,100 / yearAs an Associate Director, Bioprocess Engineering, you will lead a team of technical professionals supporting regional vaccine technology transfer, post-transfer performance, and technical readiness across assigned processes and sites, while also providing technical support to a capital project to build a manufacturing facility. Required Skills: Bioprocess Engineering, Bioprocessing, Cell Culture Process Development, GMP Operations, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Scale-Up, Pharmaceutical Manufacturing, Process Scale Up, Product Formulation, Technical Leadership, Technology Transfer, Technology Transfer Management, Vaccine Manufacturing.
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.
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.
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 Director, Quality Catalent IncSenior Director, QualityKansas City, MOThe candidate is responsible for setting the strategic direction, properly staffing, and maintaining the Quality Management Systems (QMS) to assure the KC PCH site and the campus is compliant with regulatory (21 CFR Parts 4, 201, 211, and 820), Corporate, and customer requirements. The Sr Director of Quality leads the Quality unit at the Kansas City site - Pharma/Consumer Health (PCH) and also leads the Quality organization for the Kansas City campus which includes the BioAnalytical Laboratory as well as the KC Clinical packaging and supply operation.
Senior Director, Quality CatalentSenior Director, QualityKansas City, MissouriThe candidate is responsible for setting the strategic direction, properly staffing, and maintaining the Quality Management Systems (QMS) to assure the KC PCH site and the campus is compliant with regulatory (21 CFR Parts 4, 201, 211, and 820), Corporate, and customer requirements. The Sr Director of Quality leads the Quality unit at the Kansas City site - Pharma/Consumer Health (PCH) and also leads the Quality organization for the Kansas City campus which includes the BioAnalytical Laboratory as well as the KC Clinical packaging and supply operation.
Medical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer''''s Disease) - Field Based, Central Midwest (KS, NE, IA & MO) Eisai IncMedical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer''''s Disease) - Field Based, Central Midwest (KS, NE, IA & MO)Kansas City, MO$144,300–$189,400 / yearThe impact that a Medical Science Liaison will have on the organization includes the following: a) as a representative of Eisai, a MSL will communicate key information about Eisai, the company and its hhc mission; b) provide key scientific and clinical information about Eisai's products/pipeline; serve as a conduit for communication between Eisai Research and the medical community regarding ideas for future research, and c) provide corporate value through demonstrated leadership, teamwork, participation in strategic thinking, and special projects. MSLs will be trained and certified on AD and Eisai's dementia pipeline data in order to fulfill educational gaps with KOLs/HCPs and gather medical insights to refine medical strategy and continue to close the gap on unmet educational needs for AD HCPs.
Medical Science Liaison - South Region (TX, MO, LA, OK, AR) Ipsen SAMedical Science Liaison - South Region (TX, MO, LA, OK, AR)Kansas City, MO$185,000–$215,000 / yearResponsibilities will include, but are not limited to the following: Identify, gain access to, and develop peer to peer relationships with regional and national thought leaders, active and potential study investigators, providers at academic and non-academic institutions and professional organizations within assigned geography. This role is responsible for engaging with national and regional Thought Leaders (TLs), Investigators, and Healthcare Providers (HCPs) to exchange scientific insights, support clinical research, and facilitate both clinical trial efforts and Investigator-Sponsored Studies (ISS).
Health Physicist (Radiation Safety Officer) U.S. Department of Veterans AffairsHealth Physicist (Radiation Safety Officer)Kansas City, MO$108,173–$140,627 / yearExamples of specialized experience would typically include, but are not limited to: Plans, directs, leads, and executes the radiation safety and medical health physics programs in a technical, scientific, and administrative scope of function with responsibility for all diagnostic, therapeutic and research modalities that require the use of ionizing radiation; Advises ancillary staff, researchers, technical, and medical personnel in the safe use of radioactive materials and devices producing ionizing radiation; Reviews experimental procedures specific calculations and development of risk wording, occupational dosimetry determinations for employees, and evaluation of data regarding patient absorbed radiation dose; Offers consultation and advice to other onsite and offsite senior technical experts because of the position-specific responsibilities in the various associated disciplines. You may qualify based on your experience and/or education as described below: Basic Requirement (Individual Occupational Requirement): Education: To qualify based on education for this grade level you must have a successful completion of a full 4-year course of study in an accredited college or university leading to a bachelors or higher degree that includes: natural science or engineering that included at least 30 semester hours in health physics, engineering, radiological science, chemistry, physics, biology, mathematics, and/or calculus.
Medical Records Technician (Clinical Documentation Improvement Specialist (Out/Inpatient)) U.S. Department of Veterans AffairsMedical Records Technician (Clinical Documentation Improvement Specialist (Out/Inpatient))Kansas City, MO$62,729–$81,553 / yearGS-9 Experience Requirement: In addition to the basic requirements, you must possess the following: One year of creditable experience equivalent to the journey grade level (GS-8) of a MRT (Coder-Outpatient and Inpatient); OR, An associates degree or higher and three years of experience in clinical documentation improvement (candidates must also have successfully completed coursework in medical terminology, anatomy and physiology, medical coding, and introduction to health records); OR, Mastery level certification through AHIMA or AAPC and two years of experience in clinical documentation improvement; OR, Clinical experience, such as Registered Nurse (RN), Medical Doctor (M.D.), or Doctor of Osteopathy (DO), and one year of experience in clinical documentation improvement. The Medical Records Technician (Clinical Documentation Improvement Specialist) (CDIS) is located within the Health Information Management Section (HIMS) of the Business Operations Service (BOS) at the Kansas City VA Medical Center (KCVAMC).Incumbent provides quantitative and qualitative review and analysis of medical records and encounter forms of both inpatient and outpatient encounters to ensure all diagnoses and conditions for which care is being rendered are documented by the provider in the proper sequence, and procedures have been documented and/or evaluation and management services.
Licensed Practical Nurse - PACT U.S. Department of Veterans AffairsLicensed Practical Nurse - PACTKansas City, MO$49,874–$78,163 / yearExceptions include health care education in the military service or training in the military service which is accepted by the licensing body in the jurisdiction in which the individual is licensed as qualifying for full LPN/LVN licensure will be accepted as meeting the education requirements for VHA employment or OR granted a license by a jurisdiction that does not require graduation from an approved school AND have at least one year of successful practice as an LPN/ LVN. Knowledge and skill in performing support duties for complex diagnostic tests and/or specialized practices or procedures, which include preparing the patient, assisting in the diagnostic examination, preparing and handling specialized instruments or other specialized equipment, and monitoring the patients condition before, during and following the procedure.
Medical Support Assistant (Ward Administration) - Days U.S. Department of Veterans AffairsMedical Support Assistant (Ward Administration) - DaysKansas City, MO$49,745–$64,669 / yearThe Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position. VHA locations include, but are not limited to, VA hospitals and associated clinics, community living centers (CLCs), community-based outpatient clinics (CBOCs), domiciliary units, Vet centers and VA-leased medical facilities.
Medical Review Officer (MRO) Abbott LaboratoriesMedical Review Officer (MRO)Kansas City, KS$149,300–$298,700 / yearThe position directly supports management of the MRO-A team, nursing staff, and support personnel, and plays a key role in budget oversight, quality assurance, and stakeholder engagement (including regulatory agencies, internal leadership, and external partners). WHAT YOU'LL WORK ON: Leads and supports the management of physicians and cross-functional support staff within Medical Affairs, delivering occupational medicine and drug testing services.
NewProject Engineer SIRISProject EngineerKansas City, MO$90,000–$105,000 / yearPerforming Additional Construction Related Services- Services may include but not limited to; Maintaining marked up sets of project plans and specifications for future as-built drawings; performing routine inspections of construction as work proceeds, taking action to identify work that does not conform to the contract requirement, and notifying the VA and general contractor when work requires correction; compiling, thorough site inspections, lists of defects and omissions related to the work performed and providing these lists to the contractor for correction; monitoring project financial data and budgetary cost accounting; assisting in relocation efforts; administration of construction contract change orders (preparing cost estimates, reviewing cost proposal); Submittal Review; Request for Information Review and Responses; Daily Logs of Activity; coordination of Owner supplied equipment; Operational and Maintenance data; Closeout Submittals. Responsibilities include:Monitoring Project Financial Data and Budgetary Cost Accounting - Services may include monitoring and review budgetary cost accounting; administration of construction contract change orders; maintaining spreadsheets indicating project funds allowances, obligations, payments, balances, planned expenditures, etc., assist in the documentation of the administration of construction contract change orders (preparing cost estimates, reviewing cost proposal, preparing change order packages.
Asset & Wealth Management - Renewable Energy Tax Senior Manager PricewaterhouseCoopers LLPAsset & Wealth Management - Renewable Energy Tax Senior ManagerMO$124,000–$335,000 / yearAs an Asset & Wealth Management - Renewable Energy Tax Senior Manager, you will play a pivotal role in advising clients on their local and international tax affairs, acting as a strategic consultant in business analysis, managing working capital, and profit sharing for partners. Within our Tax practice, you will navigate the complexities of the frequently changing national and international tax environment, addressing operational tax risks and structuring tax strategies for our Financial Services clients.
Thought Leader Liaison Ipsen SAThought Leader LiaisonKansas City, MO$190,000–$225,000 / yearTo be successful: the TLL team members will build close working relationships with, but not limited to: National Sales Directors, Regional Business Directors, Neuroscience Specialty Representatives, Medical Science Liaisons, Marketing teams, and Value & Access teams to ensure alignment on broader business objectives in their assigned regions. The position focuses on building and maintaining strong relationships with established and emerging thought leaders, generating actionable market insights, and driving advocacy for Ipsen's Neuroscience portfolio across Adult Spasticity, Cervical Dystonia, Pediatric Spasticity, and future anticipated indications such as Migraine.
Director, Engineering - Substation Quanta Infrastructure Solutions Group, LLCDirector, Engineering - SubstationOverland Park, KansasFull timeThe QISG team brings together Engineering, Safety, Quality, Material Procurement, QA/QC, Right-of-Way Acquisition, Scheduling, Environmental Planning, Permitting, Title and Land Management expertise that ensure outstanding results for our clients. What You'll Bring: Minimum of 15 years’ experience in the electric utility industry performing engineering related duties and/or management for high voltage electrical projects.
Director, Regional Marketing Lead (West Region) Ideaya Biosciences IncDirector, Regional Marketing Lead (West Region)KS$196,000–$242,000 / yearReporting into Commercial Strategy & Marketing, this field-based role will serve as a key commercial engagement partner responsible for developing relationships with priority thought leaders & academic centers, gathering actionable marketplace insights, supporting peer-to-peer education, and helping shape launch strategy in partnership with Marketing, Medical Affairs, Sales, Value & Access, and other cross-functional teams. The RML will play a critical role in helping IDEAYA transition to a commercial-stage organization by strengthening scientific engagement, supporting launch readiness activities, and building meaningful relationships with key stakeholders across academic and community oncology settings.
Thought Leader Liaison ImCheck Therapeutics SASThought Leader LiaisonKansas City, MO$190,000–$225,000 / yearTo be successful: the TLL team members will build close working relationships with, but not limited to: National Sales Directors, Regional Business Directors, Neuroscience Specialty Representatives, Medical Science Liaisons, Marketing teams, and Value & Access teams to ensure alignment on broader business objectives in their assigned regions. The position focuses on building and maintaining strong relationships with established and emerging thought leaders, generating actionable market insights, and driving advocacy for Ipsen's Neuroscience portfolio across Adult Spasticity, Cervical Dystonia, Pediatric Spasticity, and future anticipated indications such as Migraine.
Immunology Business Director (HS) - Mid West Incyte CorpImmunology Business Director (HS) - Mid WestKSThrough the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia. The Immunology Business Director IBD will be accountable for translating brand strategy into disciplined field execution coaching and developing high-performing Therapeutic Specialists and delivering demand generation to support launch excellence and sustained growth.
Clinical Research Nurse Coordinator University of Kansas Medical CenterClinical Research Nurse CoordinatorKS$70,200–$105,300 / yearThe position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. Job Description Summary: The Clinical Research Nurse Coordinator in the Cancer Center manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
NewGeneral Engineering & Skilled Trade Expert GTT, LLCGeneral Engineering & Skilled Trade ExpertLenexa, KSRecognized by Forbes as one of the World's Best Employers and ranked 15th globally among top biotech and pharmaceutical employers by Science Magazine, the organization employs professionals across research and development, manufacturing, clinical operations, regulatory affairs, commercial strategy, data, technology, and corporate functions who contribute directly to science that changes and extends human life. Its portfolio spans oncology, vaccines, infectious diseases, cardiometabolic health, immunology, neuroscience, and ophthalmology including what is currently the world's best-selling oncology therapy and a leading HPV vaccine with documented impact on cervical cancer rates globally.
Economic and Development Services Coordinator Clay County FloridaEconomic and Development Services CoordinatorClay County, MO$24.31–$28.44 / hourEmployees may be required to perform duties, including the employee's normal work function or other emergency support functions as deemed necessary by the County, as assigned before, during, and after hazardous weather or state of local emergency. Assist the various works units of the Economic and Development Services Department as necessary, specifically Planning and Zoning, IMS/ Special Projects Coordinator, Special Magistrate, and Code Enforcement Division as needed.
Product Management Specialist III Thermo Fisher Scientific IncProduct Management Specialist IIILenexa, KSCapable of driving improvement in business performance, directing initiatives that deliver short-, medium- and long-term growth· Familiar with working in a global/international business environment· Strong analytical and problem-solving skills· Good listener with ability to influence across teams (without direct authority)· Willing and able to travel internationally (25-35% per annum), including overnight stays· Fluent in English, additional languages a plusWhat's in it for you:· Excellent career progression opportunities with a large and growing global employer· Competitive salary, plus annual incentive bonus· Full benefits package (specifics depend on country of hire). Bachelor's degree in Microbiology, Molecular Biology, Cellular Biology or similar requiredundefined· 2+ years experience within Microbiology - either as a scientist, salesperson, or marketeer· 2-3 years of experience in Marketing or Product Management of life science or technical products and services is considered a strong advantageKnowledge, Skills, Abilities· Able to capture sharp customer insights and translate into business and product strategy and actions.·
Manager, Regional Safety AmeriCold Logistics LLCManager, Regional SafetyKansas City, MOParticipates in Regional Vice President's meetings and or calls to present Health and Safety performance statistics, discuss upcoming Health and Safety actions to improve functional performance, and proactively identifies and promptly addresses Safety and Health issues which may affect operations or may provide strategic advantage to the business. Requires the performance of work activities including reasoning, negotiating, instructing, persuading, or speaking with others; and respond appropriately to constructive feedback from executive management.
Associate Program Director Internal Medicine Prime Healthcare Services IncAssociate Program Director Internal MedicineBlue Springs, MOParticipates in resident recruitment; overseeing resident scholarly activity; ensuring the quality of clinical education, including the maintenance and development of curricula; and working directly with residents to ensure appropriate milestone development, while meeting ACGME and other regulatory body requirements. Primary Functions: The Associate Program Director is responsible for the oversight and direct supervision of the Internal Medicine Residency Program and is accountable for all program outcomes attained through the leadership and administrative oversight of the residency program.
Associate Program Director Internal Medicine St. Mary's Medical CenterAssociate Program Director Internal MedicineBlue Springs, MissouriFull timeParticipates in resident recruitment; overseeing resident scholarly activity; ensuring the quality of clinical education, including the maintenance and development of curricula; and working directly with residents to ensure appropriate milestone development, while meeting ACGME and other regulatory body requirements. The Residency Associate Program Director serves as administrative leader for St. Mary's Medical Center's graduate medical education Internal Medicine Residency Program, and assists in leading staff in the operational and financial management of the program.
Lab Coordinator, Chemistry Johnson County Community CollegeLab Coordinator, ChemistryOverland Park, KS$20.47–$26.35 / hourThis includes monitoring and answering student questions during review days, suggesting changes to alter and enhance lab exercises to improve student outcomes, communicating lab exercise schedules and room schedules to faculty, and sending weekly emails to faculty regarding lab procedures and any safety concerns. Assess and maintain safety equipment, including eye washes, safety showers, and spill kits, to ensure operability and suitability to activities performed in the lab in compliance with regulatory requirements and industry best practices.
NewKey Account Manager - Kansas City Dendreon CorporationKey Account Manager - Kansas CityKansas City, MissouriWith Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a strong Research & Development group in Seattle, WA, and a highly skilled Commercial team across the nation, Dendreon is at the forefront of cancer treatment innovation. Patient Identification, Account Activation, and Growth: Drive patient identification and account activation by understanding patient flow, referral patterns, diagnostic pathways, treatment decision points, and care team dynamics.