Responsibilities include maintaining contact with study sponsors including study initiation and follow-up documentation, managing regulatory documents and ensuring compliance with state and federal regulatory guidelines, The Clinical Research Coordinator may plan, develop, and implement start-up pro...
Contributes to coordinating qualitative research activities, including recruiting and scheduling research participants for focus groups, providing administrative support during the facilitation of focus groups, managing data storage, and coordinating research participant compensation. Supports admin...
Research areas specific to this position posting are related to medication safety in the ambulatory care setting, practice-based research, collaborative practice, and a pharmacogenomics education program. Ability to analyze results of research productivity and to recommend and design methods for imp...
The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI; Dr. Fortuna), the Center Research Supervisor, and/or the Cen...
The Assistant Clinical Research Coordinator is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including creating study specific source documents, screening for patient eligibility, data collection and analysis, ensuring protocol com...
The Clinical Research Coordinator works directly with the Principal Investigator (PI), Co-Investigators (Co-I's), postdoctoral fellows, and trainees in the performance of duties related to the support and coordination of human subjects research. The University of California, Berkeley, is one of the ...
Assistant Clinical Research Coordinator - 132908. Collaborates with physicians and researchers working in clinical research in ophthalmology at UCSD. Responsible for coordinating and managing various clinical trials simultaneously, including providing all aspects of protocol management, including pa...
Position Summary:Under the supervision of Senior Clinical Research Coordinator and Principal Investigator will coordinate and is accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. Prefer Certification from Society of C...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
The Clinical Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal Investigator (PI), assists in the operational and administrative research support of the Kaiser Permanente Northern California (KPNC) PI and KPNC Clinical Trials Operati...
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...
The Clinical Research Coordinator II works independently providing study coordination including 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 e...
The Apheresis Program Coordinator utilizes a theory-based practice to provide clinical apheresis services and direct the apheresis program coordination for stem cell transplant patients and patients with chronic hemoglobinopathies at UCSF BCH Oakland. ...
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 ...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
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 ...
The User Administration Coordinator will take the lead in coordinating these activities in collaboration with members of the User Research Administration (URA), SLAC’s Visitor User Employee (VUE) Center and its Security/Badging Office. SSRL is a national user facility, annually attracting approximat...
Coordinates plans of treatment, customer focused delivery of services, and cost effective utilization of services. Manages staff in providing delivery of high quality, patient-focused, and cost-effective pulmonary care services in a widely diverse culture across the CSA. Ensures all programs support...
Coordinates plans of treatment, customer focused delivery of services, and cost effective utilization of services. Manages staff in providing delivery of high quality, patient-focused, and cost-effective pulmonary care services in a widely diverse culture across the CSA. Ensures all programs support...
The Clinical Manager must demonstrate competence in leadership, clinical expertise, clinical supervision of program staff and personnel management, program management, program staff performance assessment, use of data, reporting, program evaluation, quality assurance, and developing and coordinating...
The goal of the Memory Program Coordinator in Training program is to successfully prepare trainees for their first management role as a Memory Program Coordinator within our senior living communities. The Memory Program Coordinator in Training program is an excellent opportunity for an Educator, Soc...
Assistant Clinical Research Coordinator- Hybrid - 133016. Experience performing clinical research duties in a clinical research environment. Certification as a Clinical Research Associate or Coordinator. Translational research is carried out every day in the hundreds of clinical trials of promising ...
In addition to tracking and scheduling, the incumbent will be responsible for handling overall project/program administration, including network and convening support; event logistics; communications both verbal and written; creation and dissemination of agendas, meeting materials and relevant resou...
Research Data Coordinator - Hybrid - 132828. As a consortium cancer center, it is a collaborative partnership between the UCSD: encompassing 14 departments (12 clinical, 2 basic sciences), 3 professional schools (School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, School of Pu...
While providing high-level professional learning the 21CSLA Research Associate will help further the understanding of how educational leaders are learning in the 21CSLA program so that the program can continue to center equity, improve work, and contribute to a larger knowledge base. Programs are no...