Main CampusDepartment:Clinical Research OperationsSchedule:Full timeHours:40Job Details:The Clinical Research Coordinator will perform clinical research activities under the general direction of the Clinical Research Supervisor/Manager and a Principal Investigator (PI) w. ...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Division of Nephrology in the Department of Internal Medicine; assists with assessing patient re...
Follow direction of clinical research coordinator or others involved in the clinical research project work. Cincinnati Children's Hospital Has Been Named: * The #1 Pediatric Hospital in the Nation - US News and World Report 2023 * One of four Medical Centers making the list of the 2022 Glassdoor Bes...
Senior Clinical Research Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the Department of Psychiatry amp; Behavioral Health in partnership with the College of Medicine (COM) Center for Clinical Research...
Serve as a resource for other clinical research professionals in all aspects of conducting a clinical trial. Cincinnati Children's Hospital Has Been Named: * The #1 Pediatric Hospital in the Nation - US News and World Report 2023 * One of four Medical Centers making the list of the 2022 Glassdoor Be...
Clinical Research Coordinator I - IGM Requisition ID 2024-52274 Category Research Overview We are seeking a Clinical Research Coordinator I to join our team. The IGM Clinical Research coordinator's primary responsibility is managing key elements of clinical research studies to meet protocol obligati...
Clinical Research Project Coordinator - Entry Level. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience. If you are looking for a fast paced, collaborative ...
The Clinical Research Coordinator (CRC) will function in a multi-faceted role and will be required to interact with Principal Investigators, Sub-Investigators, study sponsors, clinical research coordinators, contract research organizations and hospital/medical office personnel to effectively impleme...
Follow direction of clinical research coordinator or others involved in the clinical research project work. Study Conduct/ Clinical Research Practice. Assist in maintaining up-to-date and accurate written and electronic records and files to support clinical research activities. Maintain awareness of...
The Clinical Research Nurse (CRN) Works with the study physician to ensure all patients involved in a clinical research trial are managed uneventfully, safely, and as effectively as possible through their episode of care and participation in the clinical research trial, ensuring patient care is not ...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Division of General Internal Medicine's new Dissemination and Implementation Science (DIS) program within the Department of Internal Medicine; assists ...
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. ...
Clinical Research Senior Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the oversees, implements & coordinates conduct of daily activities of research studies; recruits, interviews and promotes study to...
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. ...
Serve as a resource for other clinical research professionals in all aspects of conducting a clinical trial. Communicate study related issues to investigators, sponsors, coordinating centers, study coordinators, clinical and research teams, managers and other institutions. Required for Clinical Rese...
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. ...
Working with the principal investigator and research team, coordinates implementation of research protocols. Performs research-related procedures; coordinates data collection to ensure compliance with research protocols; interfaces with Institutional Review Board (IRB) and study sponsors. Years of E...
Regulatory Affairs, Clinical Research, Medical Research, Compliance, Legal, Healthcare, Research. Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research. Clinical Research Professional, Regulatory Affairs, Star...
Certified Clinical Research Coordinator within 18 months of external hire. Study Conduct/ Clinical Research Practice. Provide oversight and guidance to research staff for all aspects of conducting a clinical trial for complex and multi-center trials. Support the data-management process for clinical ...
As a Clinical Research Coordinator, you will coordinate the compliant implementation and conduct of human subject research projects. Known for its continuous clinical trials and cancer research, the Taussig Cancer Center ensures all patients receive top-quality patient care and have access to the ne...
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Clinical Trial Supervisor and clinical Principle Investigator (PI) on multiple ongoing research studies. While the PI is ultimately responsible for the clinical trial, the CRC i...
Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials Office. The Clinical Research Coordinator. Research and Scholarship – Clinical Research – Individual Contributor/Specialized – S2. Assist with assessing patient records to identify patients who are eligible to participate in...
Summary:The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. Clinical Research Coordinator Certification (or equivalent approve...
The Clinical Research Nurse I (CRN) primary responsibility is managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Performs research activities as outlined in the protocol; im...
The Clinical Research Coordinator I is responsible for managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Understanding of medical terminology and clinical research preferre...