Principal research scientist jobs in Saint Joseph, MO - 28 jobs

Join our AI & Engineering team in transforming technology platforms, driving innovation, and helping make a significant impact on our clients' success. You'll work alongside talented professionals reimagining and re-engineering operations and processes that are critical to businesses. Your contributions can help clients improve financial performance, accelerate new digital ventures, and fuel growth through innovation. AI & Engineering leverages cutting-edge engineering capabilities to build, deploy, and operate integrated/verticalized sector solutions in software, data, AI, network, and hybrid cloud infrastructure. These solutions are powered by engineering for business advantage, transforming mission-critical operations. We enable clients to stay ahead with the latest advancements by transforming engineering teams and modernizing technology & data platforms. Our delivery models are tailored to meet each client's unique requirements. Recruiting for this role ends on 1/31/2026 Work you'll do As a Senior Consultant you will bring strong technical, functional and project management solutions to clients with a focus on achieving a high level of performance and quality through delivery of both agile and traditional projects to provide exceptional business value to users. Working within an engagement team, your responsibilities include, among others: + Managing day-to-day interactions with executive clients, stakeholders, and sponsors + Managing and delivering components of client engagements focused on identifying, designing, and implementing both technology and creative business solutions for large companies + Managing small teams to identify business requirements, functional design, process design (including scenario design, flow mapping), prototyping, testing, training, defining support procedures. Your background in technology will provide the foundation to manage these streams but also understand the technology + Creation and development of project scope and schedule. Plan and assign resources to associated tasks and deliverables + Monitoring progress of the project, identify, and quantify variances, perform required corrective actions + Managing changes to project scope, project schedule, and project costs to keep the project plan accurate, updated, as defined in the change management plan + Identifying high-level risks, assumptions, and constraints. Implement approved actions and workarounds to minimize the impact of risks on the project + Developing and maintaining communication with key project stakeholders and decision makers The team Our AI & Data practice offers comprehensive solutions for designing, developing, and operating advanced Data and AI platforms, products, insights, and services. We help clients innovate, enhance, and manage their data, AI, and analytics capabilities, ensuring they can grow and scale effectively. Across life sciences you'll find innovators who are developing therapies, treatments, devices, and cures to meet society's most pressing health challenges and deliver wellness for all. Alongside them, you'll find our leaders, the professionals of Deloitte's Life Sciences practice, who are orchestrating and delivering the business of science and health. We help drive impact through deep industry experience and insights; transformative strategies; trusted, flexible approaches; and new technologies. We help accelerate action and create connections that empower a digitally enabled, equitable future of health. Qualifications Required: + 4+ years experience with relevant professional experience + 2+ years of experience in Life Sciences Pharmaceutical R&D clinical domain to include: + introducing new technologies like GenAI, AI/ML, and automation into existing drug development and business processes. + operating model transformations; evaluation of business processes related to drug development, including workflows, key activities, inputs, outputs, and interdependencies; and analysis of clinical processes to find inefficiencies, bottlenecks, and areas for improvement. + 2+ years hands-on experience with Python, SQL and AI/ML algorithms + 1+ years experience leading workstreams within complex engagements with resources in multiple locations + Bachelor's Degree + Ability to travel up to 50% on average, based on the work you do and the clients and industries/sectors you serve + Limited immigration sponsorship may be available Preferred: + Consulting experience leading large workstreams within complex engagements + Techno-functional knowledge of clinical data flow, data architecture, and data mapping + Experience with solutions for data-driven trials and clinical development insights (ie: site burden, patient burden, study feasibility, site selection, patient recruitment and retention) + Understanding of emerging technologies, such as GenAI, and advanced data architectures is important. This includes multimodal data management, model design, Data Mesh, Data Fabric, and Data Products. + Ability to create critical collaterals for client workshops and customer interactive sessions + Presentation skills with a high degree of comfort with both large and small audiences + An advanced degree in an area of specialization The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $102,500 to $208,300. You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance. Information for applicants with a need for accommodation: ************************************************************************************************************ All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.

At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Your Role: Senior Scientist TSMS Laboratory Lead The Technical Services Manufacturing Scientist (TSMS), Senior Scientist is responsible for all aspects of processes within the Elwood, Kansas monoclonal antibody (mAb) Technical Service Manufacturing Science (TSMS) Laboratory. The Sr. Scientist will oversee the daily operations of the TSMS laboratory, ensuring experiments, tests, and research are conducted efficiently and safely. Your Responsibilities: Lead a team of scientists, ensuring high-quality, reproducible results and efficient project execution, while also managing resources. Ensure proper maintenance, calibration, and inventory of lab equipment and supplies to support timely delivery of projects. Leverage Design of Experiments (DoE) to design and execute experiments that develop, optimize, and improve manufacturing processes, ultimately enhancing cycle time, productivity, process robustness, gross margin, and production capacity. Collaborate with the site Quality Department to maintain quality requirements within the laboratory (including representing the technical service laboratory at internal and external audits). Collaborate cross-functionally with Quality Assurance, Quality Control, Engineering, Supply Chain, and Research & Development to address technical issues, foster alignment, and ensure timely project completion. What You Need to Succeed (minimum qualifications): Education: MS in Science, Pharmacy, Mechanical or Chemical Engineering, or Pharmaceutical Technology. Experience: 5+ years' experience in biotechnology process development, or manufacturing technology. Ability to lead and develop a team with strong mentoring and coaching skills & experience in mAb process development, remediation, and productivity improvement. What will give you a competitive edge (preferred qualifications): Education: Ph.D. in chemistry, engineering, or a biotechnology-related field. Highly focused and detail oriented, with high personal ethical and quality standards. Must be able to work productively in an interdisciplinary team environment. Understanding of USDA, FDA, and EU GMP regulatory standards for veterinary biologics. Ability to network and build strong, collaborative relationships across functions / geographies. Additional Information: Travel: 0-5% Location: Elwood, Kansas Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) 8-week parental leave 9 Employee Resource Groups Annual bonus offering Flexible work arrangements Up to 6% 401K matching #LI_MNLC Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Grounded in safety, quality, and ethics, our experts lead their fields with dedication, a creative spirit, and a vision for growth. We draw from more than 20 technical specialties worldwide and are devoted to fostering a community of diverse talents, backgrounds, and expertise. Here, you can apply your passion and collaborate with top environmental professionals on work that's vital to our clients and the communities they serve. Your Opportunity Join a team that's naturally committed to the environment. We are seeking an exceptionally talented and enthusiastic individual with a keen interest in the natural sciences to join our team as a full-time, mid-to-senior level lead wetland scientist in the Overland Park (Kansas City), Kansas or St. Louis, Missouri office. The ideal candidate will have strong expertise in wetland delineation, plant identification, soil characterization, and ecological fieldwork in the Midwest. This role involves up to 60% travel, data collection, and reporting related to wetland assessments and other biological surveys. The candidate will work closely with project managers, senior scientists, and staff scientists with development, coordination, and delivery of environmental permitting, assessment, or compliance documents for projects involving wind and solar electric generation facilities, electric transmission lines, natural gas pipelines, and private development projects to fulfill federal, state, and local agency requirements. Your Key Responsibilities - Delineate wetlands and other water resources in accordance with the US Army Corps of Engineers Manual and the applicable Regional Supplements. - Perform independent field studies including botanical surveys, natural community mapping, wildlife habitat assessments, and ecological impact assessments. - Support project planning and task management for field assignments. - Assist with the preparation and review of technical documents, such as wetland and waterbody delineation reports, threatened and endangered species habitat assessments, environmental assessments, environmental impact statements, permit applications and other technical reports. - Assist Project Managers/Senior Scientists by contributing technical expertise during client/regulatory meetings and proposal development. - Prepare and manage data, reports, and tables for client and agency submission. - Utilize GPS and ArcGIS Field Maps/Survey123 for data collection and mapping. - Other technical duties may include ecological restoration planning and assessment. - May also assist with other duties as assigned, including biological surveys. Your Capabilities and Credentials The ideal candidate will demonstrate strong leadership abilities with experience both leading teams and contributing as a collaborative team member. They should possess exceptional oral and written communication skills, as well as strong analytical and creative problem-solving abilities. The role also requires excellent organizational and note-taking skills, along with the ability to work independently and make sound, timely decisions in the field without direct supervision. Travel will be expected - primarily throughout the Midwest, but also within the broader U.S., and should not be assumed to be local. Education and Experience Required: - Bachelor's degree in environmental science, ecology, botany, soil science, or a related field. - 5-10 years of relevant field experience in wetland delineation and environmental assessments. - Knowledge of local/regional vegetation and soils. - Valid driver's license required. Preferred: - Master's degree in environmental science, ecology, botany, soil science, or a related field. - Experience with and proficiency in data entry using ArcGIS tools (FieldMaps and Survey123). - Wetland Professional in Training or Professional Wetland Scientist Certification. - Familiarity with state and federal environmental permitting processes. - Ability to travel extensively and work outdoors in variable weather conditions. - Task or project management experience. Typical office environment working with computers and remaining sedentary for long periods of time. Field work may include exposure to the elements including inclement weather. This description is not a comprehensive listing of activities, duties or responsibilities that may be required of the employee and other duties, responsibilities and activities may be assigned or may be changed at any time with or without notice. Stantec is a place where the best and brightest come to build on each other's talents, do exciting work, and make an impact on the world around us. Join us and redefine your personal best. \#StayInquisitive **Primary Location:** United States | MO | Kansas City **Organization:** 2277 EnvSvcs-US Great Lakes West-St Louis MO **Employee Status:** Regular **Business Justification:** New Position **Travel:** Yes **Schedule:** Full time **Job Posting:** 22/07/2025 09:07:24 **Req ID:** 1001639 Stantec provides equal employment opportunities to all qualified employees and applicants for future and current employment and prohibit discrimination on the grounds of race, colour, religion, sex, national origin, age, marital status, genetic information, disability, sexual orientation, gender identity or gender expression. We prohibit discrimination in decisions concerning recruitment, hiring, referral, promotion, compensation, fringe benefits, job training, terminations or any other condition of employment. Stantec is in compliance with laws and regulations and ensures equitable opportunities in all aspects of employment. At Stantec we are committed to ensuring our recruitment process is accessible to all. If you require reasonable adjustments to be made during the recruitment process then please inform a member of our Talent Acquisition team.

UNIVERSITY of MISSOURI-KANSAS CITY SCHOOL of MEDICINE Department of Ophthalmology Vision Research Center The University of Missouri-Kansas City is rated R1 by the Carnegie Research Classification of Institutions of Higher Education. Our research supports advances in defense, health care, public safety, technology and more aimed at a brighter and more advanced future for all. We collaborate across campus, the UM System, the region and encourage our students to participate in our research. The UMKC School of Medicine is a partner of the UMKC Health Sciences District. The District strives to be a premier academic health district, engaging in cutting-edge biomedical research and entrepreneurship, delivering state-of-the-science health care, and educating the next generation of health care professionals. UMKC provides unique opportunities for research and health care collaboration across its Schools of: Medicine, Dentistry, Nursing & Health Studies, and Pharmacy as well as University Health Physicians, regional health care institutions, and the University of Missouri System's NextGen Data Science and Analytics Innovation Center. The Vision Research Center (VRC) at UMKC is the Department of Ophthalmology's research arm, providing residents and fellows with comprehensive research opportunities, including basic research, translational research and clinical trials. ************************************************************************************************** Job Description The Vision Research Group in the department of Ophthalmology at UMKC seeks a full-time Research Scientist or Senior Research Scientist. The successful candidate will engage in research exploring the molecular mechanisms underlying ocular degeneration and engage in collaborative proteomic analysis and research studies. This position offers an opportunity to join a dynamic and collaborative research environment supported by state-of-the-art facilities at UMKC and its partner institutes in the Kansas City area. Team members are integral contributors to research publications and will have the opportunity to participate in externally funded research collaboration and translational opportunities. This is a 12-month full-time, benefit eligible, unranked academic position. Qualifications To qualify for a Research Scientist position, applicants must hold a PhD or equivalent degree and must have a minimum of two years of postdoctoral experience. To qualify for a Senior Research Scientist position, applicants must hold a PhD or equivalent degree and must have a minimum of two years of postdoctoral experience and evidence of success in obtaining external funding. Preferred qualifications include expertise in one or more of the following areas: diseases that affect the retina, including age-related macular degeneration, diabetic retinopathy and glaucoma. Anticipated Hiring Range Salary is determined by a variety of factors, including but not limited to, the individual's particular combination of education, skills, and experience, as well as organizational requirements. Your total compensation goes beyond the number on your paycheck. The University of Missouri provides generous leave, health plans, and retirement contributions that add to your bottom line. Application Materials For consideration, please apply online at ******************************** (Job Opening ID 57677). Application materials include: * Complete application on the UMKC recruitment portal including name, contact information, and questions therein. * Letter of research interest, experience, evidence of success in obtaining external funding that qualifies you as a Research Scientist or Senior Research Scientist * Curriculum Vita * List of at least 3 professional references with current contact information * Candidates will receive prior notification if references will be contacted. * Official copy of your transcripts with your highest degree earned * For credential verification Combine all materials into one PDF or Microsoft Word document and upload as your resume attachments. Limit document name to 50 characters and do not include any special characters (e.g., /, &, %, etc.). If you are experiencing technical problems during application, please email ************************** . For questions about the position, please contact Megan Florance ******************, including the Job Identification number 57677 and name of the position. Reasonable accommodations may be requested during the application and recruitment process. If you need an accommodation, please contact the Office of Equity and Title IX at **************. Application Deadline Application review will begin upon receipt. Applications will be accepted until a qualified candidate is hired. Other Information UMKC is a public, urban, R1 research university with more than 15,000 undergraduate, graduate, and professional students. It is part of the larger University of Missouri System. Our university is committed to being a model urban university that is recognized for our partnerships with surrounding urban communities to effectively foster a healthy, safe, and more economically secure quality of life. ********************* Community Information Kansas City is a diverse and vibrant community with an affordable cost of living. Our UMKC campuses are centered in the hubs of business activity, cultural arts, (some great barbeque and ethnic cuisine!) and health science research engagement for both campuses. As one of the largest cities in Missouri, we are home to national championship sports teams, a rich history of cultural arts and music, NASCAR racing, an international airport, and a community that is very engaged with and supportive of our university initiatives. Our beautiful state has rolling hills, rivers, lakes, and long bike/hiking trails for those that enjoy time in the great outdoors. Kansas City offers something for everyone! UMKC is proud to be "Kansas City's university," and the campus and its people celebrate all the characteristics of the surrounding community. To learn more about life in Kansas City and find more resources, visit VisitKC.com. Benefit Eligibility This position is eligible for University benefits. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, and educational fee discounts for all four UM System campuses. For additional information on University benefits, please visit the Faculty & Staff Benefits website at *********************************************** Equal Employment Opportunity The University of Missouri is an Equal Opportunity Employer. To request ADA accommodations, please call the Office of Equity & Title IX at ************.

Senior Associate Scientist I (Dissolution) Work Schedule: Monday - Friday, 8AM - 4:30PM 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Catalent's Kansas City (KCM) facility provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The facility is the commercial manufacturing Center-of-Excellence for accelerated development programs and roller compaction. The Senior Associate Scientist I will support the Analytics and Dissolution team for in-process, release, and stability sampling and use a variety of analytical instruments. With cutting-edge technologies and a collaborative work environment, this role offers opportunities for long-term advancement. The Role: Execute laboratory work plans/schedules developed with input from a supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC, UV/Vis, Disintegration and Dissolution. Apparatus 1, 2, 3, 5, and 6. Under direction, may perform method development, validation, and transfer activities Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs May draft technical documents such as methods or certificate of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance Assists in execution of efficiency improvement projects with guidance Trains others on laboratory techniques All other duties as assigned The Candidate: Bachelor's degree in life science or physical science is required with at least two (2) years of related work experience OR a Master's degree is required without any formal industry experience Knowledge and skills requirements include the ability to process, maintain, and interpret data, understand basic instrument troubleshooting techniques, and communicate clearly and professionally with clients and internal stakeholders Physical requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently Why you should join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 152 Hours + 8 paid holidays Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Community engagement and green initiatives Generous 401K match Company match on donations to organizations Medical, dental and vision benefits effective day one of employment Tuition Reimbursement - Let us help you finish your degree or start a new degree! WellHub program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. 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. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Job Title: Senior Data Science/Analytics Consultant JOB PURPOSE: The Senior Data Science/Analytics Consultant is responsible for the full stack of data analytics, from querying or procuring data, cleaning data, feature generation, problem formulation, error/success metric choice, machine learning/predictive model building, and translation of results into business action. This role will help advanced Transportation Insight's data strategy and data-related business decision making. The Sr. Consultant will be expected to wear multiple hats, seek out new opportunities from the business and apply technology to solve a variety of data problems across our organization. ESSENTIAL DUTIES AND RESPONSIBILITIES: Act as a cross functional consultant on data science, data analytics related efforts that span the enterprise. Identifies appropriate analytical tools and methods; uses advanced knowledge of business analysis to perform quantitative analyses and predictive modeling Be able to communicate and explain the results of more technical analyses to business partners in a digestible, visual fashion Lead strategy development for data and analytics products to ensure the program becomes pervasive throughout the organization. Develop a high performing team focused on building strong analytical, data strategy, research and business skill sets while sustaining leading employee engagement and retention. Be a stakeholder in developing and maturing the Data Science strategy PERFORMANCE METRICS: Deliver solutions according to the delivery schedule Design and architect complete end-to-end DS solutions Continuous improvement on predictive and machine learning models Conform to industry standards for quality and effective data visualization and reporting JOB REQUIREMENTS: Qualified applicants should have a Bachelor's degree in Computer Science, Information Science or related field; equivalent work experience and aptitude is acceptable in place of degree Experienced with Data Science practices and tools, such as Alteryx, R, Python, Gurobi Familiar with 3PL business and supply chain concepts Experience with ETL design and data warehousing concepts 5+ years with reporting / analytic tools such as Tableau or Cognos Experience with Oracle, MySQL and/or MS SQL Server and SQL query language required Experience with CRM tools like Salesforce Possess excellent communication and presentation skills required Strong Work Ethic **MAY PERFORM OTHER DUTIES AS ASSIGNED** WORK ENVIRONMENT: Standard office environment, usually indoors away from the elements with moderate noise. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL EFFORT: Maintain a stationary position for extended periods; move about the office, operate computers and files, as needed; and frequently communicate with others. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is required to stand, walk, and reach with hands and arms. Occasionally, the employee is required to lift boxes up to 20 pounds. SCHEDULING: This is a full-time benefits-eligible position, working Monday through Friday; 8:00 a.m. - 5:00 p.m. An employee in this position must be available to work occasionally on weekends and evenings, during peak periods. TRAVEL: Local travel is required. Out of state travel is limited, but may be required for special projects , training, and conferences. DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required.

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as a Scientist at KCAS Bio is the role for you. When you work as a Scientist II on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, dd PCR, and cell-based assays within a GLP (Good Laboratory Practice) environment. Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation. In this role, we will rely on you to: Demonstrated technical and scientific skills in molecular technologies, including DNA/RNA isolation and PCR (qPCR and dd PCR) Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level Plan and carry out all phases of assigned projects. Including- R&D, method validation, test procedure preparation, sample analysis, data calculation, interpretation & review, troubleshooting, and report preparation Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects Interact with clients and auditors as necessary Perform all aspects of the job in a way that supports the company brand, mission, vision, and values To qualify specifically for this role, you will have: Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 8 years' experience in a scientific laboratory environment Experience with design, method development, validation, and sample analysis Thorough understanding of GLP requirements and Good Documentation Practices (GDP) Experience in organizing and leading teams Manage material, equipment, and instrumentation Analyze and interpret data, prepare summary tables, and review raw data Write SOPs, study plans, and reports Communicate with clients as needed Ability to multi-task and meet deadlines Excellent verbal and written communication and organizational skills Self-motivated and driven Flexible and adaptable - able to work independently and/or in a team environment Ability to troubleshoot and problem-solve - Critical Thinking Depending on your background and qualifications, we may consider hiring you for one of three levels of Scientist roles at KCAS Bio. This will be determined during the interview process. (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU'LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to ************************** or call ************ (for TTY assistance call 711) and ask for Human Resources. IND123

Join our AI & Engineering team in transforming technology platforms, driving innovation, and helping make a significant impact on our clients' success. You'll work alongside talented professionals reimagining and re-engineering operations and processes that are critical to businesses. Your contributions can help clients improve financial performance, accelerate new digital ventures, and fuel growth through innovation. AI & Engineering leverages cutting-edge engineering capabilities to build, deploy, and operate integrated/verticalized sector solutions in software, data, AI, network, and hybrid cloud infrastructure. These solutions are powered by engineering for business advantage, transforming mission-critical operations. We enable clients to stay ahead with the latest advancements by transforming engineering teams and modernizing technology & data platforms. Our delivery models are tailored to meet each client's unique requirements. What we do Our Industry Solutions offering provides verticalized solutions that transform how clients sell products, deliver services, generate growth, and execute mission-critical operations. We deliver integrated business expertise with scalable, repeatable technology solutions specifically engineered for each sector. Who we serve T hroughout the health ecosystem, you'll find courageous and inspiring people who are committed to driving transformation, advancing health equity, and leading a well-being revolution. Where you find innovators committed to sustainable progress, you'll find Deloitte's Life Sciences & Health Care practice. Our leaders work side-by-side to orchestrate and deliver on the business of science and health. We bring trusted, flexible approaches that foster innovation, harness new technologies, and formulate consumer-driven strategies to engineer a digitally enabled, equitable future of health - starting today. Across life sciences you'll find innovators who are developing therapies, treatments, devices, and cures to meet society's most pressing health challenges and deliver wellness for all. Alongside them, you'll find our leaders, the professionals of Deloitte's Life Sciences practice, who are orchestrating and delivering the business of science and health. We help drive impact through deep industry experience and insights; transformative strategies; trusted, flexible approaches; and new technologies. We help accelerate action and create connections that empower a digitally enabled, equitable future of health. Work you'll do As an Industry Solutions Senior Consultant specializing in Life Sciences Patient Services, you will play a pivotal role in helping Patient Services clients achieve their transformation goals. Leveraging your expertise in patient services, you will interface between pharmaceutical, biotech or medical device clients and cross-functional implementation teams to identify and implement digital health solutions that improve patient outcomes. You will design, implement and optimize patient support programs, define project roadmaps and provide product and industry insights to deliver innovative solutions. The ideal candidate will be curious, analytical, and confident with a natural drive to exceed immediate project requirements and overcome obstacles. A genuine passion for the life sciences industry, combined with relationship-building, leadership, and communication skills will be critical to success. Candidates should be energized by continuous personal improvement, proactively seeking out new skills and perspectives, exhibiting openness to coaching from senior colleagues, and contributing to the development of junior staff. Key responsibilities include: + - Advise clients and Deloitte professionals (Product Owners, Designers, Developers, Architects) through the implementation of patient services technology solutions; including patient CRM, patient data & analytics solutions. + - Advise clients and Deloitte professionals on the adoption of innovative technologies to improve patient experience and operational efficiency + - Work with clients to provide product demos and help identify and design high value digital health applications supporting key patient services and healthcare use cases including defining personas, user journeys, and features + Prepare deliverables and provide leadership support to present findings and recommendations to clients and/or firm leadership + Establishing relationships with key client end users to help drive further adoption of the application throughout and at all levels of their organization Required Qualifications + Bachelor's degree in Computer Science, Healthcare Administration, Life Sciences or related field + 4 years of experience in Life Sciences Patient Services Consulting + 1 year of experience utilizing AI platforms like Chat GPT / Grok / Anthropic to conduct research and as an aid for creating presentations and project documentation + 2 years of experience with Patient Data platforms such as AWS, Databricks + 2 years of experience Patient CRM platforms; Salesforce, Veeva + 2 years of experience with PAP, Copay and/or Adherence Programs for a pharmaceutical manufacturer or patient services hub provider + 2 years of experience using Microsoft Suite (Word, Excel, Power Point) to develop and deliver professional-quality documents, reports and presentations to client stakeholders and executive level leaders + Ability to travel 50%, on average, based on the work you do and the clients and industries/sectors you serve + Limited immigration sponsorship may be available Preferred Qualifications + Advanced degree (e.g., MHA, MBA) + SQL, Power BI, Tableau data analytics skills preferred + Experience coordinating with globally located teams + Salesforce System Architect, Salesforce Application Architect, or other relevant Salesforce certifications + Experience implementing Salesforce Health Cloud or Life Sciences Cloud + SAFe, PMP, PMI, or Agile certifications + Experience defining personas, user journeys, and product features for life sciences patient services clients The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $107600 to $198400 Information for applicants with a need for accommodation: ************************************************************************************************************ All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.

**Senior Associate Scientist I (Dissolution)** + **Work Schedule:** Monday - Friday, 8AM - 4:30PM + 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Catalent's Kansas City (KCM) facility provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The facility is the commercial manufacturing Center-of-Excellence for accelerated development programs and roller compaction. The Senior Associate Scientist I will support the Analytics and Dissolution team for in-process, release, and stability sampling and use a variety of analytical instruments. With cutting-edge technologies and a collaborative work environment, this role offers opportunities for long-term advancement. **The Role:** + Execute laboratory work plans/schedules developed with input from a supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC, UV/Vis, Disintegration and Dissolution. Apparatus 1, 2, 3, 5, and 6. Under direction, may perform method development, validation, and transfer activities + Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs + May draft technical documents such as methods or certificate of analysis + Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance + Assists in execution of efficiency improvement projects with guidance + Trains others on laboratory techniques + All other duties as assigned **The Candidate:** + Bachelor's degree in life science or physical science is required with at least two (2) years of related work experience OR a Master's degree is required without any formal industry experience + Knowledge and skills requirements include the ability to process, maintain, and interpret data, understand basic instrument troubleshooting techniques, and communicate clearly and professionally with clients and internal stakeholders + **Physical requirements:** On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently **Why you should join Catalent:** + Defined career path and annual performance review and feedback process + Diverse, inclusive culture + Positive working environment focusing on continually improving processes to remain innovative + Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives + 152 Hours + 8 paid holidays + Several Employee Resource Groups focusing on D&I + Dynamic, fast-paced work environment + Community engagement and green initiatives + Generous 401K match + Company match on donations to organizations + Medical, dental and vision benefits effective day one of employment + Tuition Reimbursement - Let us help you finish your degree or start a new degree! + WellHub program to promote overall physical wellness + Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. 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. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .

UNIVERSITY of MISSOURI-KANSAS CITY SCHOOL OF DENTISTRY Oral and Craniofacial Sciences (OCS) Prof Cox's laboratory conducts both basic and translational research aimed at understanding the mechanisms coordinating normal craniofacial development and underpinning common craniofacial birth defects such as cleft lip/palate and craniofacial microsomia. The lab's research incorporates the gamut of molecular, cellular, and genetic techniques, including whole genome analysis of patients and the generation and analysis of animal models of the aforementioned disorders. Combining these approaches allows us to examine and understand the influence of both genetic variation and maternal dietary factors to disease susceptibility. The lab is somewhat unique in combining human genetic studies with expertise in 3D imaging (micro CT and Optical Projection Tomography) for the qualitative and quantitative analysis of craniofacial form in animal models. **************************************************** ***************************************************************************************************** UMKC is rated R1 by the Carnegie Research Classification of Institutions of Higher Education. Job Description The University of Missouri-Kansas City's Department of Oral & Craniofacial Sciences has an opening for a bioinformatics-trained senior research associate (any level) to join the laboratory of Prof Timothy Cox. The successful applicant will be responsible for the management and analysis of exome and whole-genome sequencing (short- and long-read) datasets from large patient cohorts encompassing both cleft lip/palate and craniofacial microsomia/microtia. They will also be responsible for working with and helping other lab members and students with their omics-related analyses, such as experiments involving RNAseq and epigenetics methods. The management and analysis of data will be conducted on both cloud-based and high-end workstation platforms. A hybrid position can also be considered, with the balance of remote and in-person work negotiable. This is a full-time, 40 hours a week, 6-month non-benefit eligible academic assignment. Qualifications Minimum requirements for the position include a doctoral degree in either the life sciences or computer sciences (with some biology training). In addition to excellent verbal and written communication skills, the successful candidate will be highly motivated, able to work independently and creatively, function as a team player, be proficient at problem solving, be willing to listen and to question, and have a deep curiosity for science. Preferred Qualifications At least 3 years of experience in mammalian genomics, epigenomics, and/or bioinformatics - particularly the analysis of whole genome sequencing and RNA sequencing datasets. Anticipated Hiring Range The anticipated hiring range for this position has been established as $5,333- $5,833 monthly. Salary is determined by a variety of factors, including but not limited to, the individual's particular combination of education, skills, and experience, as well as organizational requirements. Your total compensation goes beyond the number on your paycheck. The University of Missouri provides generous leave, health plans, and retirement contributions that add to your bottom line. Application Materials For consideration, you must apply online at ****************** click in Academic Positions (Job Opening ID 58275. Please combine all application materials, (1) a 1-page cover letter, (2) a current CV, and (3) contact information for a minimum of two referees, into one PDF or Microsoft Word document and upload as your resume attachments. Limit document name to 50 characters and do not include any special characters (e.g., /, &, %, etc.). Maximum size limit is 11MB. * If you are experiencing technical problems during application, please email ************************** . * For questions about the position, please contact ************************** including the Job Identification number 58275 and name of the position. * Reasonable accommodations may be requested during the application and recruitment process. If you need an accommodation, please contact the Office of Equity and Title IX at **************. Higher education transcripts will be required for candidates advancing as finalists. Candidates will receive prior notification if references will be contacted. A Criminal Background Check is required prior to hire. Application Deadline Applications will be accepted until a qualified candidate is hired. Other Information UMKC is a public, urban, Carnegie rated R1 research university with more than 15,000 undergraduate, graduate, and professional students. It is part of the larger University of Missouri System. Our university is committed to being a model urban university that is recognized for our partnerships with surrounding urban communities to effectively foster a healthy, safe, and more economically secure quality of life. A City on the Rise: Big City Life and Midwest Charm, Kansas City offers the best of both worlds - a vibrant, urban community with midwestern appeal and an affordable cost of living. The university is located in a Kansas City metropolitan area that is among the most entrepreneurial cities in America with a population of more than 2.4 million. Our UMKC campuses are centered in the hubs of business activity, cultural arts, (some great barbeque and ethnic cuisine!) and health science research engagement for both the Volker and Health Sciences campuses. Our community boasts championship professional athletic teams, NASCAR racing, and a rich history of music and performing arts. Our beautiful state provides rivers, lakes, biking/hiking trails and mountains for outdoor enthusiasts all within an easy drive. UMKC is proud to be "Kansas City's university," and the campus and its people celebrate all the characteristics of the surrounding community. To learn more about life in Kansas City and find more resources, visit VisitKC.com. Benefit Eligibility This position is not eligible for University benefits. Individuals in non benefit eligible positions may choose to participate in the Tax Deferred Annuity Plan (403b). For information about this plan, please visit the Faculty & Staff Benefits website at *********************************************** Equal Employment Opportunity The University of Missouri is an Equal Opportunity Employer. To request ADA accommodations, please call the Office of Equity & Title IX at ************.

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you. When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, dd PCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment. Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation. In this role, we will rely on you to: Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and dd PCR) and handling DNA/RNA Experience with procedures for the extraction and quantification of nucleic acids Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level Experience with cell culture is preferred Plan and carry out assigned experiments. Including method development, method validation, sample analysis, data calculation, interpretation & review, and troubleshooting Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects Perform all aspects of the job in a way that supports the company brand, mission, vision, and values To qualify specifically for this role, you will have: Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment Experience with design, method development, validation, and sample analysis Experience with GLP requirements and Good Documentation Practices (GDP) Manage material, equipment, and instrumentation Analyze and interpret data, prepare summary tables, and review raw data Assist with the preparation and review of SOPs, study plans, and reports Ability to multi-task and meet deadlines Excellent verbal and written communication and organizational skills Self-motivated and driven Flexible and adaptable - able to work independently and/or in a team environment Ability to troubleshoot and problem-solve - Critical Thinking (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU'LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to ************************** or call ************ (for TTY assistance call 711) and ask for Human Resources. IND123

Job DescriptionPerforming critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you. When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, dd PCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment. Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation. In this role, we will rely on you to: Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and dd PCR) and handling DNA/RNA Experience with procedures for the extraction and quantification of nucleic acids Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level Experience with cell culture is preferred Plan and carry out assigned experiments. Including method development, method validation, sample analysis, data calculation, interpretation & review, and troubleshooting Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects Perform all aspects of the job in a way that supports the company brand, mission, vision, and values To qualify specifically for this role, you will have: Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment Experience with design, method development, validation, and sample analysis Experience with GLP requirements and Good Documentation Practices (GDP) Manage material, equipment, and instrumentation Analyze and interpret data, prepare summary tables, and review raw data Assist with the preparation and review of SOPs, study plans, and reports Ability to multi-task and meet deadlines Excellent verbal and written communication and organizational skills Self-motivated and driven Flexible and adaptable - able to work independently and/or in a team environment Ability to troubleshoot and problem-solve - Critical Thinking (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU'LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to ************************** or call ************ (for TTY assistance call 711) and ask for Human Resources. IND123 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Department: SOM KC Family Medicine * ---- Family Medicine Postdoctoral Fellowship - Family Medicine Job Family Group: Professional Staff The Postdoctoral Fellow will engage in advanced, mentored research at the intersection of implementation science, cost-effectiveness analysis, community-engagement and global health. Working closely with Dr. Sarah Kessler and other clinical and research faculty in the Department of Family Medicine and Community Health, the Fellow will contribute to the design, execution, and dissemination of research focused on improving the delivery, quality, and sustainability of health interventions in resource-constrained settings. The position emphasizes professional development and preparation for independent research careers. The Fellow will receive structured mentorship in implementation science frameworks, mixed-methods research, and economic evaluation, and will be encouraged to develop a distinct scholarly trajectory, build interdisciplinary collaborations, and present findings at national and international conferences. Additional opportunities include mentoring junior trainees and participating in team-science activities, consistent with institutional policies. This role is well suited for candidates with prior research experience and a strong interest in implementation science, cost-effectiveness analysis, and global health. Job Description: Job Duties Outlined Research Overview * Work independently and collaboratively on research projects. * Conduct quantitative and qualitative data analysis. * Assist with development of grant proposals and scientific manuscripts. * Maintain a current Laboratory Notebook, documenting all calculations, work, experiments, and other pertinent research information. Expectations * Read literature articles, develop new ideas, and assimilate the information into project design/interpretation. * Lead and support implementation science studies. * Support and engage in research efforts in community clinics and service organizations. * Contribute to economic and cost-effectiveness analyses. * Collaborate with domestic and international partners. * Develop manuscripts for peer-reviewed publication. * Develop proposals for external funding. Required Qualifications Education: PhD in public health, sociology, mental health, psychology or related field. This position requires a formal degree in the cited discipline area(s) to ensure that candidates have advanced knowledge, analytical skills and professional competencies necessary to perform the duties of the position. The level of degree is commonly recognized as the standard qualification for similar roles in the public and private sector, ensuring that the university remains competitive with industry aligned practices, enhances collaboration with external partners, and supports the delivery of services and programs that meet professional and market-driven expectations. Preferred Qualifications Work Experience: * Experience with implementation research, cost or cost-effectiveness analyses, and/or global or low-resource settings. * Experience with quantitative and/or mixed methods research. Skills * Collaboration. * Computer skills. * Communication. * Analytical skills. Required Documents * Resume/CV * Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: Regular Time Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range: $63,905.00 - $90,000.00 Minimum $63,905.00 Midpoint $76,953.00 Maximum $90,000.00

Department:SOM KC Physical Medicine and Rehabilitation ----- Physical Medicine and RehabilitationPosition Title:Post Doctoral Fellow - Physical Medicine and RehabilitationJob Family Group: Professional Staff Summary:The Postdoctoral Fellow in the Guggenmos Lab within the Department of Physical Medicine and Rehabilitation will play a key role in advancing neuroscience research through experimental and analytical work. This position is responsible for conducting neurophysiology experiments, performing large-scale analysis of neural datasets, and contributing to scientific publications. The Fellow will also assist with animal care in support of ongoing studies and collaborate with team members to drive high-quality, impactful research.: Job Duties Outlined: Research Overview: Design and conduct experiments and interpret data under the mentorship of the Principal Investigator (PI). Work independently and collaboratively on research projects. Assist with development of grant proposals and scientific manuscripts. Maintain a current Laboratory Notebook, documenting all calculations, work, experiments, and other pertinent research information. Conduct neurophysiology experiments. Perform large dataset analysis of neural data. Assist with lab animal care. Assist with publishing scientific journal articles. Expectations: The Postdoc will be expected to complete research projects under the guidance of the faculty mentor, record and interpret the results of their experiments in an (electronic) laboratory notebook, prepare publication-quality manuscripts (including figures and tables) and publish in peer-reviewed literature. Read literature articles, develop new ideas, and assimilate the information into his/her project design/interpretation. Dissemination of studies: Interact on a regular basis with their PI, faculty mentor and members of the laboratory to discuss experimental design and interpretation of results. Present research aims and findings at department seminars and at local and national scientific meetings. Write and publish their results as first author in abstracts, manuscripts, and posters. Compliance: Attend and maintain compliance on all orientation and training sessions designated by the University and the Department, understand and follow IACUC and biosafety protocols, and attend departmental seminars and regular lab meetings. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible. Required Qualifications: Education: PhD in Bioengineering or Neuroscience or related field. This position requires a formal degree in the cited discipline area(s) to ensure that candidates have advanced knowledge, analytical skills and professional competencies necessary to perform the duties of the position. The level of degree is commonly recognized as the standard qualification for similar roles in the public and private sector, ensuring that the university remains competitive with industry aligned practices, enhances collaboration with external partners, and supports the delivery of services and programs that meet professional and market-driven expectations. Work Experience: Two years of experience in Neuroscience. Preferred Qualifications: Work Experience: Four years experience in Neuroscience Required Documents: Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: RegularTime Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range:$63,477.00 - $90,000.00 Minimum $63,477.00 Midpoint $76,739.00 Maximum $90,000.00

Department:SOM KC Internal Medicine - Nephrology and Hypertension ----- Medicine - Nephrology and HypertensionPosition Title:Post Doctoral Fellow - Internal Medicine (Nephrology) Job Family Group: Professional Staff Summary:The Post Doctoral Fellow in the Department of Internal Medicine, Division of Nephrology will work in a research laboratory focusing on kidney and vascular disease-related outcomes research. Research activities will center on the study of hypertension, kidney disease, diabetes, and other cardio-renal risk factors and their impact on cognitive function, brain health, and quality of life in older adults. This position will encompass clinical, epidemiological, and translational research.: Job Duties Outlined: Research Overview: Design and conduct research studies and interpret data under the mentorship of the Principal Investigator (PI). Work independently and collaboratively on research projects. Participate in the design and execution of observational studies, clinical trials, and implementation research related to vascular and kidney disease. Conduct data collection, management, and analysis using clinical and population-based datasets. Contribute to the development of study protocols, manuals of procedures, and regulatory documentation. Assist with preparation of grant proposals and scientific manuscripts. Maintain accurate and up-to-date research documentation in accordance with study and institutional requirements. Expectations: The Post Doctoral Fellow will be expected to complete research projects under the guidance of the faculty mentor; analyze and interpret study results; prepare publication-quality manuscripts, including tables and figures; and publish findings in peer-reviewed journals. Review and synthesize relevant scientific literature to inform study design and interpretation. Develop research questions and contribute to study design and analytic strategies. Engage regularly with the PI, faculty mentors, and research team to discuss study progress, design considerations, and interpretation of results. Present research aims and findings at departmental seminars and at local and national scientific meetings. Prepare abstracts, posters, and manuscripts as first author when appropriate. Compliance: Attend and maintain compliance with all required University and Department orientation and training sessions; adhere to IRB, data security, and research compliance requirements; and participate in departmental seminars and regular research meetings. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. Required Qualifications Education: PhD or equivalent experience in public health, psychology, dementia, geriatrics, hypertension, kidney disease, or other health-related field. This position requires a formal degree in the cited discipline area(s) to ensure that candidates have the foundational knowledge and skill set required to perform the duties of the position. The level of degree is based on accreditation requirements, institutional standards of academic and professional excellence, alignment with peer institution benchmarks, and contributes to the credibility and effectiveness of the role within the university community. Preferred Qualifications Work Experience: A record of publications or scientific writings as demonstrated by application materials. Experience with SPSS or other statistical software. Skills Organization Communication Critical thinking Problem solving Attention to detail Interpersonal skills Collaboration Computer skills Required Documents Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: RegularTime Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range:$63,477.00 - $90,000.00 Minimum $63,477.00 Midpoint $76,739.00 Maximum $90,000.00

Department: SOM KC Internal Medicine - Nephrology and Hypertension * ---- Medicine - Nephrology and Hypertension Post Doctoral Fellow - Internal Medicine (Nephrology) Job Family Group: Professional Staff The Post Doctoral Fellow in the Department of Internal Medicine, Division of Nephrology will work in a research laboratory focusing on kidney and vascular disease-related outcomes research. Research activities will center on the study of hypertension, kidney disease, diabetes, and other cardio-renal risk factors and their impact on cognitive function, brain health, and quality of life in older adults. This position will encompass clinical, epidemiological, and translational research. : Job Duties Outlined: Research Overview: Design and conduct research studies and interpret data under the mentorship of the Principal Investigator (PI). * Work independently and collaboratively on research projects. * Participate in the design and execution of observational studies, clinical trials, and implementation research related to vascular and kidney disease. * Conduct data collection, management, and analysis using clinical and population-based datasets. * Contribute to the development of study protocols, manuals of procedures, and regulatory documentation. * Assist with preparation of grant proposals and scientific manuscripts. * Maintain accurate and up-to-date research documentation in accordance with study and institutional requirements. Expectations: The Post Doctoral Fellow will be expected to complete research projects under the guidance of the faculty mentor; analyze and interpret study results; prepare publication-quality manuscripts, including tables and figures; and publish findings in peer-reviewed journals. * Review and synthesize relevant scientific literature to inform study design and interpretation. * Develop research questions and contribute to study design and analytic strategies. * Engage regularly with the PI, faculty mentors, and research team to discuss study progress, design considerations, and interpretation of results. * Present research aims and findings at departmental seminars and at local and national scientific meetings. * Prepare abstracts, posters, and manuscripts as first author when appropriate. Compliance: Attend and maintain compliance with all required University and Department orientation and training sessions; adhere to IRB, data security, and research compliance requirements; and participate in departmental seminars and regular research meetings. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. Required Qualifications Education: PhD or equivalent experience in public health, psychology, dementia, geriatrics, hypertension, kidney disease, or other health-related field. * This position requires a formal degree in the cited discipline area(s) to ensure that candidates have the foundational knowledge and skill set required to perform the duties of the position. The level of degree is based on accreditation requirements, institutional standards of academic and professional excellence, alignment with peer institution benchmarks, and contributes to the credibility and effectiveness of the role within the university community. Preferred Qualifications Work Experience: * A record of publications or scientific writings as demonstrated by application materials. * Experience with SPSS or other statistical software. Skills * Organization * Communication * Critical thinking * Problem solving * Attention to detail * Interpersonal skills * Collaboration * Computer skills Required Documents * Resume/CV * Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: Regular Time Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range: $58,656.00 - $80,000.00 Minimum $58,656.00 Midpoint $69,328.00 Maximum $80,000.00

Department:SOM KC Family Medicine ----- Family MedicinePosition Title:Postdoctoral Fellowship - Family MedicineJob Family Group: Professional Staff Summary:The Postdoctoral Fellow will engage in advanced, mentored research at the intersection of implementation science, cost-effectiveness analysis, community-engagement and global health. Working closely with Dr. Sarah Kessler and other clinical and research faculty in the Department of Family Medicine and Community Health, the Fellow will contribute to the design, execution, and dissemination of research focused on improving the delivery, quality, and sustainability of health interventions in resource-constrained settings. The position emphasizes professional development and preparation for independent research careers. The Fellow will receive structured mentorship in implementation science frameworks, mixed-methods research, and economic evaluation, and will be encouraged to develop a distinct scholarly trajectory, build interdisciplinary collaborations, and present findings at national and international conferences. Additional opportunities include mentoring junior trainees and participating in team-science activities, consistent with institutional policies. This role is well suited for candidates with prior research experience and a strong interest in implementation science, cost-effectiveness analysis, and global health.Job Description: Job Duties Outlined Research Overview Work independently and collaboratively on research projects. Conduct quantitative and qualitative data analysis. Assist with development of grant proposals and scientific manuscripts. Maintain a current Laboratory Notebook, documenting all calculations, work, experiments, and other pertinent research information. Expectations Read literature articles, develop new ideas, and assimilate the information into project design/interpretation. Lead and support implementation science studies. Support and engage in research efforts in community clinics and service organizations. Contribute to economic and cost-effectiveness analyses. Collaborate with domestic and international partners. Develop manuscripts for peer-reviewed publication. Develop proposals for external funding. Required Qualifications Education: PhD in public health, sociology, mental health, psychology or related field. This position requires a formal degree in the cited discipline area(s) to ensure that candidates have advanced knowledge, analytical skills and professional competencies necessary to perform the duties of the position. The level of degree is commonly recognized as the standard qualification for similar roles in the public and private sector, ensuring that the university remains competitive with industry aligned practices, enhances collaboration with external partners, and supports the delivery of services and programs that meet professional and market-driven expectations. Preferred Qualifications Work Experience: Experience with implementation research, cost or cost-effectiveness analyses, and/or global or low-resource settings. Experience with quantitative and/or mixed methods research. Skills Collaboration. Computer skills. Communication. Analytical skills. Required Documents Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: RegularTime Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range:$63,905.00 - $90,000.00 Minimum $63,905.00 Midpoint $76,953.00 Maximum $90,000.00

Department:SOM KC Biochemistry ----- Research StaffPosition Title:Postdoctoral Fellow - BMB Research StaffJob Family Group: Professional Staff Summary:A post-doctoral fellow position is available immediately in the NIH-funded group of Dr. Chad Slawson. The candidate selected for the position will work as part of a diverse research group, encompassing undergraduate, graduate, and postdoctoral level scientists, employing cellular biology, molecular biology, mass spectrometry, and biochemical approaches focusing on understanding the role of O-GlcNAc in Alzheimer's disease. The fellow will work on multiple projects in the lab while developing new lines of inquiry. Postdoctoral scholars at the University of Kansas Medical Center are individuals who have received their terminal degree and who have opted to pursue further training in a postdoctoral appointment. Postdoctoral scholarship is a time-limited appointment, the primary purpose of which is to provide research and/or scholarly training for an academic or research career. A postdoctoral scholar at KUMC is expected to: Participate in a full-time regimen of advanced training and research, train under the supervision of a faculty research mentor who will provide the opportunity for collaborative and independent research, as well promote publication of findings and preparation of research grants as determined by a mutual agreement between the postdoctoral scholar and the mentor, participate in relevant academic activities related to the preparation for a career in research or academia, participate in the University's Individual Development Plan policy for postdoctoral scholars, have a PhD or equivalent terminal degree (such as MD, DVM, PsyD, PharmD, etc.), and candidates should have strong English skills and demonstrate an ability to write and communicate with a scientific audience. Candidates must be able to independently plan, multi-task and complete projects. Ideally, the fellow will be expected to design and execute experiments, analyze data, write and prepare independent grant applications and manuscripts for scientific publications, and supervise graduate students.: Key Roles and Responsibilities: Primary duties will include cellular microscopy, protein immunoblotting, maintenance of cell cultures, and DNA isolation and analysis. Attend all orientation and training sessions designated by the University and Department, attend departmental seminars and attend regular lab meetings. Provide laboratory training for new students and fellows in the lab. Will participate in various research projects under the guidance of the faculty supervisor, record and interpret the results of their experiments in a laboratory notebook. Interact on a regular basis with faculty and other members of the laboratory to discuss experimental design and interpretation of results. Develop and maintain lab guidelines for specific studies as directed by lab supervisor. Order supplies and negotiate prices on lab consumables. Follow established quality control and quality assurance policies and procedures, including appropriate documentation. Serve as lab safety person as needed. Dispose of biohazardous materials, chemical waste, sharps and other potentially hazardous materials according to policy, and strictly adheres to safety and biosafety control procedures. Calibrate, maintain, and operate equipment keeping appropriate documentation. Report malfunctions to supervisor. Maintain adequate inventory of lab kits and reagents. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. Required Qualifications Work Experience: 2 years of experience in either cellular biology, molecular biology, or biochemistry. Education may be substituted for experience on a year for year basis. Preferred Qualifications Education: Bachelor's in biology, chemistry, or medicine or other science/medicine-related area. Work Experience: Previous lab experience working with tissue culture. Previous lab experience working with protein expression and purification. Skills Written and verbal communication skills. Computer skills, data management, and organizational skills. Required Documents: Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: RegularTime Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range:$63,477.00 - $90,000.00 Minimum $63,477.00 Midpoint $76,739.00 Maximum $90,000.00

Department:SOM KC Radiation Oncology ----- Radiation OncologyPosition Title:Post Doc Fellow - ONC Radiation OncologyJob Family Group: Professional Staff Summary:Postdoctoral scholar is expected to perform studies in Dr. Subhrajit Saha's laboratory under NIH funded project to examine immune regulation of intestinal epithelial regeneration, development of radiation countermeasure. Candidate also expected to participate in other ongoing projects such as gut microbiome in radiation response of intestinal and pulmonary tissue, examine the role of macrophages in gastrointestinal cancer. To learn more about ongoing research in Saha laboratory please visit ****************************************************************************************************************************** Key Roles and Responsibilities Perform research and interpretation of experimental results and analysis of data Design and perform animal experiments to related to radiation biology and immunology Generation of data and its analysis for the preparation of published papers, as well as assistance on grant submissions and other documentation necessary for laboratory compliance This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. Required Qualifications: Education: PhD in the Biological Sciences. Work Experience: 5 year of lab training in the field of regenerative medicine or immunology or cancer biology or radiation biology, which included running experiments, synthesizing data and writing manuscripts. This position requires a formal degree in the cited discipline area(s) to ensure that candidates have the foundational knowledge and skill set required to perform the duties of the position. The level of degree is based on accreditation requirements, institutional standards of academic and professional excellence, alignment with peer institution benchmarks, and contributes to the credibility and effectiveness of the role within the university community. Preferred Qualifications: Work Experience: Experience in mice genetics, animal studies including tail vein injections, flowcytometry, transcriptomic analysis. Skills: Technical skills. Required Documents: Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. ************************************************** Employee Type: RegularTime Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range:$58,656.00 - $80,000.00 Minimum $58,656.00 Midpoint $69,328.00 Maximum $80,000.00