Under the supervision of the Assistant Director of Business Development & Technology, incumbent is responsible for managing recruitment of potential research participants for clinical trials at the UCI Center for Clinical Research, within Good Clinical Practice (GCP) guidelines. The UCI Center for C...
Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America Clinical Develop...
See Professorial Series (Adjunct, Clinical X, HS Clinical, In Residence, Ladder Rank) and Professor of Teaching Series - Health Sciences Compensation Plan. Pediatric Neonatology Research -Clinical X Series, Associate or Professor Rank. The University of California Irvine (UCI) School of Medicine, De...
Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Assist with ma...
The AoUSCC led by UCI is a part of the larger research structure for the All of Us Research Program and the Genetic Epidemiology Research Institute (GERI) efforts including UCI faculty and researchers in furthering the science of precision medicine using the All of Us data. Broad knowledge of clinic...
Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America Clinical Develop...
Essential Functions Delivers all relevant services/tasks in support of the planning and implementation of quality driven clinical trials, in line with established targets and strategies Implements proactive risk identification and mitigation planning for assigned clinical trial sites, leveraging Ris...
A minimum of 12 months experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite). Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. ...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for...
The goals of the fellowship are identification of appropriate areas of research activities, research methodology and experimental design, preparation of grant proposals, scientific writing: preparation of abstracts for scientific meetings and manuscripts for peer review journal publication and admin...
Clinical research experience from a sponsor. Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred. We generate extensive clinical evidence to demonstrate the effectiveness and safety of ou...
Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America Clinical Develop...
We are seeking an experienced and dedicated Research Site Manager to oversee the operations of our clinical research site. Oversee the day-to-day operations of the clinical research site, ensuring that all activities comply with study protocols, regulatory requirements, and Good Clinical Practice (G...
Under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The UCI Center for Clinical Research (CCR) is driven to improve health and w...
The Clinical Research Field Monitor is responsible for compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Experienced with Good Clinical Practice (GCP) in conduct of clinical studies. Preferably certified as a Clinical Research ...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
This professional will report to Clinical Science and External Research (CSER) Leaders in the management of assigned clinical projects for the Cardiovascular Group to support the development of the evidence generation and dissemination strategy of assigned products, manage clinical studies, execute ...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
The Clinical Research Specialist (CRS) is responsible for supporting and/or conducting clinical study activities and basic data collection at clinical sites, as well as managing assigned clinical projects & operations, including pre-monitoring activities, data entry, inventory management, device pro...
The RNC provides support, coordination and leadership for FDA regulated research including drug/device/biologic studies that may involve industry sponsored Phase I, II, III and IV clinical trials, government funded clinical research and investigator initiated clinical research. The Research Nurse Co...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
This is an entry-level position that would be suitable for a phlebotomist who is looking to enter the field of clinical research. Site Management Organization (SMO) that provides administrative and operational support to help facilitate Phase II-IV clinical trials. We conduct research in high-qualit...