NewPediatric Gastroenterologist Norton HealthcarePediatric GastroenterologistLouisville, KYNORTON CHILDREN’S GASTROENTEROLOGY, affiliated with the UofL School of Medicine, and part of Norton Children’s Medical Group, is seeking a board-certified/board-eligible pediatric gastroenterologist to join our team of physicians and staff providing a broad range of clinical gastrointestinal services. The current pediatric gastroenterology service covers the 300-bed free-standing, full-service Norton Children’s Hospital and two local outpatient clinics.
NewEpileptologist Norton HealthcareEpileptologistLouisville, KY$2,018–$2,022Comprehensive epilepsy center with fellowship-trained neurologists, neurosurgeons and neuropsychologists, as well as advanced practice providers, a social services coordinator and an epilepsy patient navigator. Opportunity to participate in dedicated specialty clinics (ketogenic diet and neurogenetics), a monthly multidisciplinary refractory epilepsy conference and weekly neuroscience case conferences.
NewClinical Laboratory Scientist United States ArmyClinical Laboratory ScientistLexington, KYBenefits may include: ★ Repayment of qualified education loans to lending institution, paid annually over a maximum of three years while serving ★ Travel opportunities, to include humanitarian missions ★ Up to 30 days of paid vacation earned annually ★ Enrollment in a military retirement system that blends the traditional legacy retirement pension with a defined contribution to service members’ Thrift Savings Plan account ★ No- to low-cost medical and dental care for you and your family ★ Commissary and post exchange shopping privileges ★ Possible specialized training assistance and monthly stipend while enrolled in an accredited residency program ★ Specialized training to become a leader in medicine Eligibility Requirements ★ Must have a bachelor’s degree from a DA-approved accredited college or university ★ Must have a certification in Medical Technology/Medical Laboratory Science by the American Society for Clinical Pathology (ASCP) with one-year work experience ★ Must be a U.S. citizen for Active Duty ★ Must have a permanent U.S. residency to serve in the Army Reserve Have questions or want more information? Outstanding Benefits When you join the Army Medical Service Corps, you’ll be making a difference in the lives of our Soldiers and the country at large while gaining access to invaluable opportunities, like supporting humanitarian missions, leadership training and a competitive benefit package.
Clinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews Days 8a-430p Norton HealthcareClinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews Days 8a-430pLouisville, KentuckyFull timeAdditionally, 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.
Clinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews Days Norton Healthcare FoundationClinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews DaysLouisville, 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.
Assistant Clinical Research Director Trusted Medical PLLCAssistant Clinical Research DirectorLouisville, KentuckyThe Clinical Research Director will provide leadership and oversight for the activities of the Trusted Medical Research Institute, including the management of multiple clinical studies from start-up through closeout. The CRD will provide scientific and strategic direction, oversee staff and resources, manage stakeholder relationships, and support the development and implementation of new clinical trials.
NewClinical Research Nurse II University of LouisvilleClinical Research Nurse IILouisville, KYThe CRN 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 CRN demonstrates leadership in adhering to ethical principles in the conduct of clinical trials in order to protect study subjects and data integrity. Clinical Research at the Brown Cancer Center includes early phase, novel treatment, multi-centered, cooperative and intergroup trials, multi-institutional pharmaceutical trials, and single- or multi-centered investigator-initiated trials.
NewClinical Research Coordinator - CRC Trusted Medical PLLCClinical Research Coordinator - CRCLouisville,, KYTrusted Medical is seeking an experienced Clinical Research Coordinator to support our growing national clinical research program serving Veterans, active-duty military personnel, and communities nationwide. Strong team player with the ability to collaborate effectively with clinical teams, Veterans, military personnel, sponsors, vendors, and leadership .
Clinical Research Coordinator I Mass General BrighamClinical Research Coordinator ILexington, KentuckyFollowing established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc. and maintaining and updating data generated by the study. The successful candidate will be comfortable working independently to manage study activities while communicating effectively with participants, investigators, and research team members to ensure smooth study operations.
Clinical Research Coordinator I University of KentuckyClinical Research Coordinator ILexington, KY$23.18–$38.25 / hourThe Clinical Research Coordinator I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Job Title Clinical Research Coordinator I Requisition Number RE55745 Working Title CRC I (DATA) Department Name 7H024:MCC - CLINICAL RESEARCH ORG Work Location Lexington, KY Grade Level 45 Salary Range $23.18-38.25/hour
Clinical Research Coordinator DelRicht ResearchClinical Research CoordinatorLouisville, KYClinical Research Coordinator's Main Objective: Overall, the Clinical Research Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies: Patients have a fun, positive and comfortable experience at our clinic. Maintaining Physician Trust - You are seen as a go to, knowledgeable resource to our physicians including ensuring the physician is well informed of their schedule and updated on all current clinical trial patients and protocols.
Principal Investigator (MD/DO) – Clinical Research – Louisville, KY The IMA GroupPrincipal Investigator (MD/DO) – Clinical Research – Louisville, KYLouisville, KentuckyOur Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. You'll have the opportunity to support the launch and growth of a new research site while benefiting from IMA's established workflows, experienced research teams, and clinical research infrastructure.
Senior Research Coordinator IQVIASenior Research CoordinatorLexington, KentuckyJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits.
Clinical Research Associate II Allen SpoldenClinical Research Associate IILouisville, KentuckyConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Covington, KentuckyRemoteFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Research Finance Analyst Baptist Healthcare System IncResearch Finance AnalystLexington, KYKey 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. The Research Financial Analyst oversees all financial functions within the Clinical Trial Management System (CTMS), including the development, maintenance, and reconciliation of study budgets, as well as the accurate recording, allocation, and tracking of study-related financial transactions.
Client Relationship Associate Director, Connected Devices PM (Clinical Research) IQVIA Holdings IncClient Relationship Associate Director, Connected Devices PM (Clinical Research)Lexington, KY$90,200–$251,200 / yearTo communicate with project teams and Business Development to ensure excellent delivery to clients and consistency across studies, including alliance and portfolio management, implementation of best practices, harmonization, and development of client-specific performance improvement projects, and to facilitate escalation management. Assist the Business Development team with RFP (request for proposal)/RFI (request for information) review for assigned accounts, working closely with the internal teams and the client.
Senior Research Coordinator IQVIA Holdings IncSenior Research CoordinatorLexington, KY$44,300–$110,500 / yearJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You'll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities - from patient recruitment and informed consent to regulatory documentation and site audits.
RN Research Nurse SEH Saint Elizabeth Medical CenterRN Research NurseEdgewood, KentuckyPerforms duties within the scope of the appropriate state Nurse Practice Act and conducts research studies according to the Office for Human Research Protections (OHRP) and US Food and Drug Administration (FDA) regulations and guidelines. Obtains patient biological specimens or works with SEH laboratory / SEH clinical nursing staff to obtain laboratory specimens (blood, urine, saliva, etc.).
RN Research Nurse St. Elizabeth HealthCareRN Research NurseEdgewood, KYPerforms duties within the scope of the appropriate state Nurse Practice Act and conducts research studies according to the Office for Human Research Protections (OHRP) and US Food and Drug Administration (FDA) regulations and guidelines. Obtains patient biological specimens or works with SEH laboratory / SEH clinical nursing staff to obtain laboratory specimens (blood, urine, saliva, etc.).