NewDialysis Clinical Manager Registered Nurse - RN Fresenius Medical CareDialysis Clinical Manager Registered Nurse - RNLagrange, KYAs the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease. We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.
Clinical Recruiter/Coordinator | ON-SITE Vaco LLCClinical Recruiter/Coordinator | ON-SITElouisville, KY$24–$25 / hourDetermining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. This role will be responsible for sourcing, screening, interviewing, and coordinating the hiring process for positions such as Registered Nurses (RNs), Licensed Practical Nurses (LPNs), Medical Assistants, Therapists, Technicians, and other healthcare professionals.
NewRN Clinical Manager - Home Health BrightSpring Health ServicesRN Clinical Manager - Home HealthJeffersonville, INOffice Location: Jeffersonville, INCoverage area:Jeffersonville, IN Schedule:Full Time How YOU will benefit: Guide and support a team of dedicated nurses and clinicians delivering high-quality, 1:1 patient care in the home setting. As a Home Health Clinical Manager, You will: Conducts/participates in quarterly quality improvement meetings, reviews pertinent available data, identifies trends, and oversees the implementation of improvement plans.
Clinical Research Coordinator V University of LouisvilleClinical Research Coordinator VLouisville, KYManages all aspects of the trial including timely and accurate CRF completion for each study subject, timely data entry in CTO trial management system, timely and appropriate reporting adverse events (AEs) and resolution of queries; and reviews and maintains source documentation for all CFR entries including clinic visit notes, lab data and procedure reports. Informs faculty of potential eligibility, educates patients and family members on appropriate clinical trials available; develops resources and materials for patient/family teaching; reviews and verifies all relevant source documentation in subject's record before subjects are enrolled; and documents protocol exemptions and deviations as appropriate.
NewSenior Clinical Research Associate - CNS - Midwest/Southeast (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - Midwest/Southeast (Remote)KYRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Clinical Research Nurse, CAHRDS Operations Days 8a-430p Grant Funded Evening and Weekend requirements. Norton HealthcareClinical Research Nurse, CAHRDS Operations Days 8a-430p Grant Funded Evening and Weekend requirements.Louisville, KentuckyFull timeThe CRN functions as a liaison between patients, investigators, local clinic, sponsors, Norton Healthcare Office of Research Administration and their research management team. Certified Clinical Research Associate OR Certified Clinical Research Coordinator OR Certified Clinical Research Professional.
Clinical Research Coordinator I OraClinical Research Coordinator ILouisville, KentuckyPerform 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.
Coordinator, Clinical Research, CAHRDS Operations, Days 8a-430p Grant Funded- Evening and Weekend Requirements Norton HealthcareCoordinator, Clinical Research, CAHRDS Operations, Days 8a-430p Grant Funded- Evening and Weekend RequirementsLouisville, KentuckyFull timeThe 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 II Iterative Scopes Inc.Clinical Research Coordinator IINew Albany, INThis role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success. Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
Clinical Appeals Manager, Medical Plaza II University of Louisville Physicians IncClinical Appeals Manager, Medical Plaza IILouisville, KYClinical support will include pre-bill edits, payment denials, and pre/post-payment audits from insurance carriers or designated third party vendors as related issues such as medical necessity, experimental determinations, medically unlikely edits, non-covered services, and/or documentation. Additional Job Description: UofL Health Core Expectation: At UofL Health, we expect all our employees to live the values of honesty, integrity and compassion and demonstrate these values in their interactions with others and as they deliver excellent patient care by: Honoring and caring for the dignity of all persons in mind, body, and spirit.
Clinical Research Coordinator I Ora, Inc.Clinical Research Coordinator ILouisville, KYPerform 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.
Coordinator, Clinical Research, NCIRP Research Operations, Days Norton HealthcareCoordinator, Clinical Research, NCIRP Research Operations, DaysLouisville, KentuckyFull timeThe 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.
Coordinator, Clinical Research, NCIRP Research Operations, St Matthews Days Norton HealthcareCoordinator, Clinical Research, NCIRP Research Operations, St Matthews DaysLouisville, KentuckyFull timeThe 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 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 Nurse I University of LouisvilleClinical Research Nurse ILouisville, KYEssential Duties and Responsibilities: Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility. This position will work with the Principal Investigator (PI) to develop a recruitment plan for each assigned protocol and identify potential sources for subjects by establishing appropriate networks to support referrals.
Clinical Pharmacist, South Hospital, PRN University of Louisville Physicians IncClinical Pharmacist, South Hospital, PRNShepherdsville, KYThe Clinical Pharmacist actively participates in multidisciplinary patient-care rounds, medication order evaluation and verification, drug distribution, technician supervision, and clinical services including medication histories, pharmacokinetic dosing, drug information requests, and patient counseling to ensure the best medication therapy outcomes. Job Description Summary: UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center.
Clinical Pharmacist, Brown Cancer Center, Blood Cancers, Cellular Therapies and Transplant University of Louisville Physicians IncClinical Pharmacist, Brown Cancer Center, Blood Cancers, Cellular Therapies and TransplantLouisville, KYMajor job responsibilities include: medication order evaluation (to include but not limited to appropriateness and effectiveness) and verification, drug distribution support, technician supervision, clinical intervention, formulary management, and resource for nursing and physician medication related inquiries. Job Description Summary: UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center.
Clinical Pharmacist, Medical Center South, 6:30a-5:30p University of Louisville Physicians IncClinical Pharmacist, Medical Center South, 6:30a-5:30pShepherdsville, KYThe Clinical Pharmacist actively participates in multidisciplinary patient-care rounds, medication order evaluation and verification, drug distribution, technician supervision, and clinical services including medication histories, pharmacokinetic dosing, drug information requests, and patient counseling to ensure the best medication therapy outcomes. Shift: Job Description Summary: UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center.
Clinical Pharmacist, Mary and Elizabeth Hospital, 9p-7a University of Louisville Physicians IncClinical Pharmacist, Mary and Elizabeth Hospital, 9p-7aLouisville, KYThe Clinical Pharmacist actively participates in multidisciplinary patient-care rounds, medication order evaluation and verification, drug distribution, technician supervision, and clinical services including medication histories, pharmacokinetic dosing, drug information requests, and patient counseling to ensure the best medication therapy outcomes. Job Description Summary: UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center.
Clinical Pharmacist, Jewish Hospital, Critical Care, 12p-10p, 7 on/7 off University of Louisville Physicians IncClinical Pharmacist, Jewish Hospital, Critical Care, 12p-10p, 7 on/7 offLouisville, KYThe Clinical Pharmacist actively participates in multidisciplinary patient-care rounds, medication order evaluation and verification, drug distribution, technician supervision, and clinical services including medication histories, pharmacokinetic dosing, drug information requests, and patient counseling to ensure the best medication therapy outcomes. Job Description Summary: UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center.