Clinical Research Assistant, Clinical Support Operations, Leatherman Spine Research Days 8a-430p Norton Healthcare FoundationClinical Research Assistant, Clinical Support Operations, Leatherman Spine Research Days 8a-430pLouisville, KYAdditionally, the CRA is responsible to maintain research medical equipment; accurately maintain logs; perform protocol-related tasks as assigned (within scope of practice); inventory, store, order and maintain study-related equipment/ supplies. Certified Clinical Data Manager OR Certified Clinical Research Associate OR Certified Clinical Research Coordinator OR Certified Clinical Research Professional OR Certified Medical Assistant OR Certified Tumor Registrar.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateKYRemoteli>Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate II ICON PlcClinical Research Associate IILouisville, KYFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
Clinical Research Nurse I University of KentuckyClinical Research Nurse ILexington, KY$25.01–$41.25 / hourThis position will ensure effective data flow related to human clinical studies, including patient evaluation/assessment, registration, compilation and submission of data, monitoring of study compliance and other responsibilities associated with the coordination of human clinical studies. Job Title Clinical Research Nurse I Requisition Number RE54581 Working Title CRN I Department Name 7H024:MCC - CLINICAL RESEARCH ORG Work Location Lexington, KY Grade Level 46 Salary Range $25.01-41.25/hour
Clinical Research Nurse, Norton Cancer Institute - Downtown Norton Healthcare FoundationClinical Research Nurse, Norton Cancer Institute - DowntownLouisville, KYp>Desired: • Master Degree • Certified Clinical Research Associate • Certified Clinical Research Coordinator • Certified Clinical Research Professional. The CRN functions as a liaison between patients, investigators, local clinic, sponsors, Norton Healthcare Office of Research Administration and their research management team.
Clinical Research Coordinator I OraClinical Research Coordinator ILouisville, Kentuckyul>Competencies and Personal Traits:What We Do:Execution Excellence: Ability to set goals, create structure and maintain a focused and collaborative approach to the delivery of timely and high-quality work. Why We Do It:Seek Meaning and Purpose and a Desire to be Part of Something Bigger than Yourself: Crave being part of a team that works together under shared values to achieve significant positive impact in the wider world.
Clinical Research Nurse II University of LouisvilleClinical Research Nurse IILouisville, KYThe CRNII facilitates compliances with the research protocol and Good Clinical Practice guidelines; uses multiple communication styles and methods to facilitate the effective coordination of clinical trials across disciplines and clinics, acting as a liaison between the principle investigator, sponsoring agent, study patients, referring physicians, pharmacist, statisticians and other members of the research team; takes leadership in ensuring an effective informed-consent process and study subject safety for the duration of the trial; ensures compliance with protocol procedures, assessments and reporting requirements; assists physicians in ensuring adequate source documentation and data-collection that validate the integrity of the clinical trial; assist in enhancing recruitment of study participants, helping with the design and implementation of recruitment strategies for identifying and assessing patients who may be eligible for a clinical trial; and the CRNII demonstrates leadership in adhering to ethical principles in the conduct of clinical trials in order to protect study subjects and data integrity. Essential Duties and Responsibilities: • Coordinates all aspects of clinical trials initiation to ensure full compliance with sponsors and FDA, indirectly supervises data management with any aspect of protocol initiation coordination and data management (i.e., informed consent revisions, submissions to IRB, completion of research forms).
Clinical Research Coordinator I Ora IncClinical Research Coordinator ILouisville, KYp>Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
NewClinical Research Coordinator II University of KentuckyClinical Research Coordinator IILexington, KY$25.01–$41.25 / hourp>Job Title Clinical Research Coordinator II Requisition Number RE54893 Working Title CRC II (Clinical) Department Name 7H024:MCC - CLINICAL RESEARCH ORG Work Location Lexington, KY - Onsite Grade Level 46 Salary Range $25.01-41.25/hour To be considered you must fully complete the online application being sure to only put one (1) job title for each entry (multiple job titles for one employer must have separate entries), the # of hours worked per week and your ending salary.
Clinical Research Coordinator I University of KentuckyClinical Research Coordinator ILexington, KY$22.73–$37.50 / hourp>The Clinical Research Coordinator I is responsible for coordinating study activities, collecting and maintaining research data, ensuring protocol compliance, assisting with patient recruitment and enrollment, monitoring participant safety, and supporting regulatory and study documentation requirements. Job Title Clinical Research Coordinator I Requisition Number RE54870 Working Title CRC I (CRO) Department Name 7H024:MCC - CLINICAL RESEARCH ORG Work Location Lexington, KY Grade Level 45 Salary Range $22.73-37.50/hour
Clinical Research Coordinator II Shriners Hospitals for ChildrenClinical Research Coordinator IILexington, KYReporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SC International Headquarters, the CRC II provides support in accordance with SC's policies and procedures, SC's hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. Actively collaborates with applicable headquarters departments, including Research Programs, Legal, and Compliance related to protocol reviews, IRB submissions, sponsored contracts, material transfers, data use agreements, and HIPAA compliance for projects conducted within SHC.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsLexington, KY$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
STEPS Clinical Research Assistant University of KentuckySTEPS Clinical Research AssistantLexington, KYJob Title STEPS Clinical Research Assistant Requisition Number TE09322 Department Name 7H150:BEHAVIORAL SCIENCE Work Location Lexington, KY Salary Range $21/hour Type of Position Temporary Position Time Status Full-Time Required Education Required Related Experience Required License/Registration/Certification Physical Requirements. Job responsibilities include telephone screening, data entry, conducting subject interviews, conducting daily research sessions, assisting in the coordination of research studies, recruitment of research subjects, and assisting with the analysis of data for scientific publication.
Clinical Research Coordinator Baptist Healthcare System IncClinical Research CoordinatorLexington, KYThe CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of the patient. Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements.
NewClinical Research Coordinator Level 1 Baptist Healthcare System IncClinical Research Coordinator Level 1Louisville, KYThe CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of the patient. Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIALexington, KYb>Deprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85. .
Clinical Research Nurse II University of KentuckyClinical Research Nurse IILexington, KY$27.48–$45.33 / hourp>The Clinical Research Nurse will involved in research design, oversee ethical and participant safety issues, development and regulation of investigational drugs and devices, be responsible for clinical study operations, management of the study site, and all project related data and informatics. Maintain confidentiality; ensure work is detailed, accurate and completed in a timely manner; lift, push, and/or pull objects up to 50lbs; stand or walk with objects up to 25lbs; and possible exposure to radiation, cuts/punctures, bloodborne/airborne pathogens, and/or challenging individuals.
Clinical Research Coordinator I Shriners Hospitals for ChildrenClinical Research Coordinator ILexington, KYReporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and to the Research Programs Office at SHC International Headquarters, the CRC1 provides support in accordance with SHC's policies and procedures, SHC's hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. Actively collaborates with applicable headquarters departments, including Research Programs, Legal, and Compliance related to protocol reviews, IRB submissions, sponsored contracts, material transfers, data use agreements, and HIPAA compliance for projects conducted within SHC.
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsLexington, KY$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Clinical Research Associate (PhD Candidates) Medpace Holdings IncClinical Research Associate (PhD Candidates)Louisville, KYp>Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Coordinator, Clinical Research, Norton Cancer Institute - Downtown Norton Healthcare FoundationCoordinator, Clinical Research, Norton Cancer Institute - DowntownLouisville, KYThe CRC functions as a liaison between patients, investigators, local clinic, sponsors, Norton Healthcare Research Office and their research management team. The CRC represents Norton Healthcare Research as assigned clinics within the community.
Clinical Research Coordinator IV University of LouisvilleClinical Research Coordinator IVLouisville, KYUnder the direction of the BCC Clinical Trial Office leadership and in collaboration with a Research Nurse (RN) or Clinical Research Coordinator (CRC), the Clinical Research Coordinator IV assists in the coordination of daily activities related to the conduct of oncology clinical trials. The Clinical Research Coordinator IV is expected to attend Multi-disciplinary clinics, conferences, workshops, and other learning opportunities in order to stay informed in the relevant areas and maintain competency in coordinating clinical research studies.
Clinical Research Coordinator V University of LouisvilleClinical Research Coordinator VKYp>Position Description: Working under the direction of the clinical Principal Investigators (PI), in the Department of Surgical Oncology, the Clinical Research Coordinator V is responsible for the enrollment, active accrual, implementation, facilitation and coordination of daily clinical trials activities and plays a critical role in the conduct of multiple clinical research studies. The Clinical Research Coordinator V works collaboratively with investigators, multidisciplinary clinical entities, sponsors, monitors and regulatory entities to ensure the safety of study participants, the efficiency of study operations and the timely completion of studies.
Operations Finance Director, Clinical Research Central Laboratory Thermo Fisher Scientific IncOperations Finance Director, Clinical Research Central LaboratoryHighland Heights, KY$145,000–$170,000 / yearAcross Financial Planning & Analysis, Tax, Treasury, Financial Reporting, Audit, Investor Relations, Strategy & Corporate Development, and Accounting, our global Finance organization provides diverse opportunities to shape business outcomes, drive innovation, and build meaningful career experiences. This is an opportunity to play a pivotal role in shaping the financial strategy of a global clinical research organization, directly supporting the delivery of life-changing therapies while developing talent and driving meaningful business impact!
Research Project Coordinator Baptist Healthcare System IncResearch Project CoordinatorLexington, KYThe Project Coordinator acts as a liaison to ensure the efficient, compliant, and timely initiation of clinical research studies by facilitating feasibility reviews, including completion of sponsor questionnaires and data-driven site assessments, coordinating pre-study and site initiation activities, and overseeing study onboarding processes. The Project Coordinator will serve as a key resource within the Baptist Health Research (BHR) program, providing assistance to internal Baptist providers, research leadership, and staff, as well as to external research sponsors, collaborators, and vendors, for the setup and ongoing oversight of study procurement and onboarding across a diverse clinical research portfolio.
Coord Research St. Elizabeth HealthcareCoord ResearchEdgewood, KYWork directly with principal investigator to assist in the design of recruitment strategies, communication plan, patient safety monitoring plan, ensure compliance with protocol guidelines and requirements of regulatory agencies, including required documentation and record retention. Obtains patient biologic specimens or works with SEH laboratory/SEH clinical nursing staff to obtain laboratory specimens (blood, urine, saliva, etc.).
Research Administrator Associate University of KentuckyResearch Administrator AssociateLexington, KYRemotep>A successful candidate will have the ability to understand, interpret, and research complex and varied regulations, think critically and work collegially in order to successfully resolve questions and issues for faculty, staff, and colleagues, communicate timely and professionally to a range of individuals, have the ability to multitask and prioritize, have a strong attention to detail, and have a willingness to be a lifelong learner. Job Title Research Administrator Associate Requisition Number RE54534 Working Title Department Name 40130:Sponsored Projects Administration Work Location Lexington, KY Grade Level 45 Salary Range $47,278-78,000/year Type of Position Staff Position Time Status Full-Time Required Education.
Research Administrative Coordinator University of KentuckyResearch Administrative CoordinatorLexington, KYRemote$43,805–$70,075 / yearJob Title Research Administrative Coordinator Requisition Number RE54578 Working Title Department Name 40133:Clinical Research Support Office Work Location Lexington, KY Grade Level 44 Salary Range $43,805-70,075/year Type of Position Staff Position Time Status Full-Time Required Education. Services provided by the CRSO include maintaining a clinical trial management system (CTMS), conducting coverage analysis, developing study budgets, negotiating payment terms with sponsors, and regulatory services.
Research Project Manager University of KentuckyResearch Project ManagerLexington, KY$52,021–$85,800 / yearResponsibilities include planning and implementing the study protocol across recruitment clinics; coordinating participant screening, enrollment, and retention; managing and monitoring REDCap data collection for all study visits; monitoring study-related budget items; managing regulatory planning and IRB compliance under PI supervision; and coordinating study tasks with other team members. Job Title Research Project Manager Requisition Number RE54784 Working Title Research Project Manager Department Name 7H800:PSYCHIATRY Work Location Lexington, KY Grade Level 46 Salary Range $52,021-85,800/year Type of Position Staff Position Time Status Full-Time Required Education.
NewSenior Director, Research & Development - Healthcare Nutrition (Dysphagia Focus) Lyons MagnusSenior Director, Research & Development - Healthcare Nutrition (Dysphagia Focus)Walton, KYOur portfolio serves patients across acute care, long-term care, and home settings, and we are rapidly expanding our healthcare presence to better reach and provide the highest level of care for our healthcare providers, caregivers, and patients. Lead the full lifecycle development of healthcare nutrition products, including thickened liquids, texture-modified foods, oral nutritional supplements, and hydration solutions for dysphagia patients.
NewSenior Director, Research & Development – Healthcare Nutrition (Dysphagia Focus) Lyons Magnus LLCSenior Director, Research & Development – Healthcare Nutrition (Dysphagia Focus)Walton, KYOur portfolio serves patients across acute care, long-term care, and home settings, and we are rapidly expanding our healthcare presence to better reach and provide the highest level of care for our healthcare providers, caregivers, and patients. Lead the full lifecycle development of healthcare nutrition products, including thickened liquids, texture-modified foods, oral nutritional supplements, and hydration solutions for dysphagia patients.
Pediatric Clinical Psychologist - Eating Disorders Norton HealthcarePediatric Clinical Psychologist - Eating DisordersLouisville, Kentuckyul>Primary responsibilities include evaluating and treating children/adolescents with eating disorders and their families primarily in an outpatient medical setting; assisting in further developing programs; implementing empirically-based treatment modalities such as CBT, DBT, FBT, and ACT; and serving as a consultant to Norton Healthcare medical staff.. Pediatric or child clinical psychologist with training and experience in pediatric eating disorders services .
NewLead, Data Quality/Integrity - Clinical Abstraction Operations Humana IncLead, Data Quality/Integrity - Clinical Abstraction OperationsKYRemote$106,900–$147,000 / yearp>Work at Home Requirements To ensure Home or Hybrid Home/Office employees' ability to work effectively, the self-provided internet service of Home or Hybrid Home/Office employees must meet the following criteria: At minimum, a download speed of 25 Mbps and an upload speed of 10 Mbps is required; wireless, wired cable or DSL connection is suggested. To ensure Home or Hybrid Home/Office employees' ability to work effectively, the self-provided internet service of Home or Hybrid Home/Office employees must meet the following criteria: At minimum, a download speed of 25 Mbps and an upload speed of 10 Mbps is required; wireless, wired cable or DSL connection is suggested.
Research Finance Analyst Baptist Healthcare System IncResearch Finance AnalystLexington, KYem> Experience in clinical research finance, healthcare finance, or related field Demonstrated experience working with clinical trial budgets, financial systems, and research billing processes Work Experience Relevant Work Experience Education If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now! Key responsibilities include building study budgets in the CTMS; payment coding; processing deposits and allocating funds within the CTMS; maintaining the accounts receivable tracker; generating invoices for subject visits, administrative fees, and all other billable items outlined in the Clinical Trial Agreement (CTA); and submitting invoices for industry-sponsored studies and all applicable federal studies through CTSU OPEN.
Research Scientist- Remote Community Health Center IncResearch Scientist- RemoteKYRemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.
NewAssistant Professor Term - Comparative Medicine Research Unit (CMRU) University of LouisvilleAssistant Professor Term - Comparative Medicine Research Unit (CMRU)Louisville, KYShared program responsibilities will include but not be limited to: 1) assisting in the management of UofL animal facilities including clinical care and health monitoring associated with rodent quarantine, transgenic animals, large animal models and medical/educational research, 2) contributing to program planning, design, renovation/construction, and operation of rodent animal facilities, 3) completing special administrative projects as assigned by the Assistant Director or the Associate Vice President for Animal Welfare, and 4) participation in a broad range of regulatory activities associated with animal care and use including those related to IACUC, AAALAC, OLAW, and the USDA. This position will have a faculty appointment in the University of Louisville School of Medicine as an Assistant Professor (Term) and ability to apply for promotion to Associate Professor (Term) according to School of Medicine requirements.
Research Coordinator V University of LouisvilleResearch Coordinator VLouisville, KYOpportunities to assist with grant applications may also be possible and may include pre-award and post-award responsibilities such as completion of forms, formatting and verification of accuracy of documentation, verification of application completeness, assistance with budget development and post-award budgetary management, and other post-award project management tasks. It is generally anticipated that the individual will spend about 20 hours per week engaged in the wet lab and the remaining 20 hours/week coordinating study activities, including participant recruitment and data curation.
Clinical Manager, Gastroenterology (GI) Customer Success Cardinal HealthClinical Manager, Gastroenterology (GI) Customer SuccessField, IllinoisRemoteSpecialty Networks leverages the Power of its Network, represented by over 10,000 providers, to help independent physician practices, industry, wholesalers/distributors, payers, and policymakers improve patient outcomes. We are a distributor of pharmaceuticals and specialty products; a global manufacturer and distributor of medical and laboratory products; an operator of nuclear pharmacies and manufacturing facilities; and a provider of performance and data solutions.
Research Data Scientist CommonSpirit HealthResearch Data ScientistBardstown, KYp>Our commitment to serve the common good is delivered through the dedicated work of thousands of physicians, advanced practice clinicians, nurses, and staff; through clinical excellence delivered across a system of 140 hospitals and more than 2,200 care centers serving 24 states. Analysis and Performance Improvement - Uses computer software to analyze clinical and financial data to help identify and understand opportunities to improve outcomes, reduce costs, and improve satisfaction with clinical care.
Pediatric Clinical Geneticist Norton HealthcarePediatric Clinical GeneticistLouisville, KentuckyResponsibilities: NORTON CHILDREN’S GENETICS CENTER, affiliated with the UofL School of Medicine, is seeking a boardcertified/ board-eligible physician in both pediatrics and clinical genetics. Job Responsibilities: The physician is responsible for recording a detailed medical history of each patient in the electronic medical record, including, but not limited to, chief complaint, present condition, individual history, and family history.
Pharmacist Clinical Staff/UKHC University of KentuckyPharmacist Clinical Staff/UKHCLexington, KY$104,697–$156,062 / yearp>Job Title Pharmacist Clinical Staff/UKHC Requisition Number RE54813 Working Title Pharmacist Clinical Staff/UKHC - Hematology/Oncology Department Name H3330:Pharmacy Services Work Location Lexington, KY Grade Level 14 Salary Range $104,697-156,062/year Type of Position Staff Position Time Status Full-Time Required Education. Pharmacists contribute to the scholarly productivity of the enterprise through clinical research, quality improvement, presentations, publications, etc., and uphold UK Healthcare core values and maintain effective teamwork with pharmacists, residents, technicians, interns, physicians, nurses, allied health staff, and others.
Cell Therapy- Field Clinical Advisor Midwest (AR, MO, KS, NE, IA, KY) AstraZeneca PlcCell Therapy- Field Clinical Advisor Midwest (AR, MO, KS, NE, IA, KY)KY$197,000–$295,000 / yearIn addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Capture applicable field insights (feasibility, operational bottlenecks, patient pathways) and deliver them to global and local partners to lead early risk identification and inform protocol/process adjustments.
NewPharmacist Clinical Staff/Shift-BSD/UKHC University of KentuckyPharmacist Clinical Staff/Shift-BSD/UKHCLexington, KY$114,697–$156,062 / yearp>Job Title Pharmacist Clinical Staff/Shift-BSD/UKHC Requisition Number RE54918 Working Title Pharmacist Clinical Staff/Shift-BSD/UKHC Department Name H3330:Pharmacy Services Work Location Lexington, KY Grade Level 14 Salary Range $114,697-156,062/year Type of Position Staff Position Time Status Full-Time Required Education. Provide pharmaceutical care to patients admitted to Inpatient neurosurgery, neurology, stroke and medicine intensive care services through actively participating on patient care rounds, contacting and conferring with physicians and other healthcare practitioners to optimize medication therapy and reviewing and perfecting medication orders.
Clinical Instructor, Assistant, Associate, or Professor in Social Work University of KentuckyClinical Instructor, Assistant, Associate, or Professor in Social WorkLexington, KYp>Job Title: Clinical Instructor Assistant Associate or Professor in Social Work Requisition Number: FE04720 Working Title: Faculty Position Department Name: 8T110 College of Social Work Work Location: Lexington, KY Type of Position: Full-Time Tenure Track Status: Non-Tenure Track. To continue to advance our support infrastructure for CoSW, we invite applicants for a 12-month, non-tenure eligible, open rank position in the Clinical Title Series to begin as early as Fall 2025 or Spring 2026.
Clinical Therapist SPARC RecoveryClinical TherapistRussell Springs, Kentuckydiv>Job Responsibilities:Complete and maintain accurate records or reports regarding the clients' histories and progress, services provided, or other required information. Interview clients, review records, and confer with other professionals to evaluate individuals' mental and physical condition and to determine their suitability for participation in a specific Residential/IOP/OP/SOP or After Care program.
Clinical Sales Specialist, Structural Heart - Structural Interventions (Lexington, KY) Abbott LaboratoriesClinical Sales Specialist, Structural Heart - Structural Interventions (Lexington, KY)Lexington, KY$78,000–$156,000 / yearp>This particular role is focused on Abbott's Amplatzer Congenital offering which encompasses atrial septal defects (ASD), patent ductus arteriosus (PDA) and ventricular septal defects (VSD), and patent foramen ovale (PFO). In this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures.
Principal Clinical Specialist, Coronary Renal Devernation - Louisville, KY Medtronic PlcPrincipal Clinical Specialist, Coronary Renal Devernation - Louisville, KYLouisville, KYRemoteThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
NewPediatric Clinical Geneticist - Louisville, Ky Norton Medical GroupPediatric Clinical Geneticist - Louisville, KyLouisville, KYtd>Call or Text Recruiter: (270) 635-0060kennisha.walker@nortonhealthcare.org?subject=Pediatric%20Clinical%20Geneticist%20Career%20Opportunity%20. About Norton Children's .NewClinical Coordinator RN Baptist Healthcare System IncClinical Coordinator RNCorbin, KYli>Required certifications/training include BLS, ACLS, Basic Cardiac Arrhythmia, NIH Stroke Certification, 12 Lead Training, Glucometer Training, Aegis/DY, and Nurse Wound Care within established departmental timeframes. The Clinical Coordinator functions as a clinical pathway, population-based clinician responsible for promoting patient safety and high-quality patient care through clinical leadership, education, consultation and modeling.NewClinical Account Associate, Kentucky Tempus AI IncClinical Account Associate, KentuckyKYTempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician).1234Resume ResourcesFree Resume TemplatesFree Resume BuilderSimilar Job SearchesClinical Documentation Specialist JobsClinical Specialist JobsNursing JobsMedical JobsRemote HealthcareEntry Level HealthcareGet noticed by top employers!Upload your resume to let employers know you're open to Clinical Research job opportunities. Plus, receive relevant job recommendations in your inbox.Send Us Your ResumeCreate A Free Account
NewClinical Coordinator RN Baptist Healthcare System IncClinical Coordinator RNCorbin, KYli>Required certifications/training include BLS, ACLS, Basic Cardiac Arrhythmia, NIH Stroke Certification, 12 Lead Training, Glucometer Training, Aegis/DY, and Nurse Wound Care within established departmental timeframes. The Clinical Coordinator functions as a clinical pathway, population-based clinician responsible for promoting patient safety and high-quality patient care through clinical leadership, education, consultation and modeling.
NewClinical Account Associate, Kentucky Tempus AI IncClinical Account Associate, KentuckyKYTempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician).