- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... timelines.CORE JOB FUNCTIONS + Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research… more
- University of Miami (Miami, FL)
- …planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies . This role assists in the day-to-day operations of clinical ... research protocol implementation, and carries out study coordination duties from protocol initiation to ... study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works… more
- University of Miami (Miami, FL)
- …in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies . This role assists in the day - to - day operati ons ... of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close - out according to… more
- University of Miami (Hollywood, FL)
- …and evaluating of multiple clinical research protocols. This role manages multiple studies ' daily operations, carries out study coordination duties from protocol ... development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study 's integrity, and mentors less experienced Clinical… more
- University of Miami (Miami, FL)
- …and evaluating of multiple clinical research protocols. This role manages multiple studies ' daily operations, carries out study coordination duties from protocol ... development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study 's integrity, and mentors less experienced Clinical… more
- University of Miami (Miami, FL)
- …and evaluating of multiple clinical research protocols. This role manages multiple studies ' daily operations, carries out study coordination duties from protocol ... development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study 's integrity, and mentors less experienced Clinical… more
- University of Miami (Miami, FL)
- …planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies . This role assists in the day-to-day operations of clinical ... research protocol implementation and carries out study coordination duties from protocol initiation to ... study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works… more
- IQVIA (Durham, NC)
- …US based **JOB OVERVIEW** The main purpose of this role is to manage the assigned IRT studies in a way that ensures all patients get the study drug on time and ... study and data integrity are maintained from study go live to close out. An important aspect...to develop the relationship with the client while the study is ongoing in such a way that they… more
- System One (Diamondhead, MS)
- …(PI) provides medical leadership and overall oversight for cardiology-focused clinical research studies conducted at the Diamondhead, MS site. This PRN role ensures ... that all study activities are performed in compliance with ICH-GCP, FDA,...the main point of contact for sponsors, CROs, and study monitors. Key Responsibilities + Lead and oversee all… more
- Johns Hopkins University (Baltimore, MD)
- …Sciences is seeking a **_Clinical Research Coordinator_** to conduct clinical trials, clinical studies , and discover new ways to prevent and treat diseases and other ... Coordinator administratively coordinates clinical protocol implementation, typically for a single study . Will ensure the efficient logistical implementation of the … more
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