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.
Clinical Research Assistant, Norton Cancer Institute Research Operations Downtown or St. Matthews Days 8a-430p Norton HealthcareClinical Research Assistant, Norton Cancer Institute Research Operations Downtown or 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.
FSP Clinical Research Associate 2 - Central Region Fortrea IncFSP Clinical Research Associate 2 - Central RegionKYRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
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.
NewClinical Research Coordinator Trusted Medical PLLCClinical Research CoordinatorLouisville, KYJoin a growing clinical research organization where your expertise will directly support high-quality research, improved study access, and meaningful outcomes for Veterans, active-duty service members, and communities nationwide. This position plays a key role in coordinating clinical research activities, maintaining regulatory compliance, supporting study participants, and ensuring trials remain on schedule from initiation through closeout.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceKYTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedKYTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
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.
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.
Clinical 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.
Clinical Research Nurse I University of KentuckyClinical Research Nurse ILexington, KY$25.01–$41.25 / hourJob 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 This 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.
Client Relationship Associate Director, Connected Devices PM (Clinical Research) IQVIA Holdings IncClient Relationship Associate Director, Connected Devices PM (Clinical Research)Lexington, KY$90,200–$251,200 / yearTo communicate with project teams and Business Development to ensure excellent delivery to clients and consistency across studies, including alliance and portfolio management, implementation of best practices, harmonization, and development of client-specific performance improvement projects, and to facilitate escalation management. Assist the Business Development team with RFP (request for proposal)/RFI (request for information) review for assigned accounts, working closely with the internal teams and the client.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIALexington, KYDeprecated : preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85 .
NewClinical 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 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.
NewAssistant 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.
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.
Clinical Research Coordinator II University of KentuckyClinical Research Coordinator IILexington, KY$25.51–$42.08 / hourJob Title Clinical Research Coordinator II Requisition Number RE55693 Working Title Department Name 7H854:OPHTHALMOLOGY & VISUAL SCIENCE Work Location Lexington, KY Grade Level 46 Salary Range $25.51-42.08/hour This position will also be responsible for helping investigators to identify potential study patients as well as ensure that all study files and documentation is accurate and follows GCP guidelines.
NewSTEPS 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.