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...
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. Certified Clinical Research Professional certification...
Experience performing clinical research duties in a clinical research environment. Experience performing clinical research duties in a clinical research environment. Assistant Clinical Research Coordinator- Hybrid - 133016. Responsible for coordinating and managing clinical trials including providin...
Clinical Research Regulatory Coordinator. Bachelor’s degree in a health science field; certification in clinical research (e. Minimum of 2-3 years of experience in clinical research with a focus on regulatory compliance. Strong knowledge of clinical research regulatory requirements, including FDA re...
Responsible for coordinating and managing various clinical trials simultaneously, including providing all aspects of protocol management, including patient recruitment and scheduling, screening for patient eligibility, data acquisition, collection and analysis, interpreting research protocols, ensur...
If you are an experienced study coordinator looking for a leadership role in a dynamic clinical research setting, we would love to hear from you!. The Senior Study Coordinator will work closely with investigators, research staff, and external partners to support high-quality, timely, and reliable da...
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...
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 ...
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 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 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...
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 II (CTRC-II) is a position with demonstrated proficiency in coordinating clinical trial research tasks which, under the clinical direction of the Principal Investigator (PI), provides research, operational, and administrative support to the Kaiser Permanente N...
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...
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...
Sierra Donor Services (SDS) is looking for a dynamic and enthusiastic team member to join us to save lives!! Our mission at DCIDS is to save lives through organ donation and we want professionals on our team that will embrace this important work!! Sierra Donor Services is seeking a Clinical Manager...
PBL has immediate openings for a Research Associate in the. The Research Associate is expected to perform under minimal supervision. Research Associates also contribute to general laboratory operations including animal health monitoring, equipment maintenance, and maintaining a clean and organized l...
The Ronda lab at the Innovative Genomics Institute at UC Berkeley is seeking a highly motivated Assistant Project Scientist to join our multidisciplinary lab. Our research focuses on mapping the human-microbiome interactome using Systems Biology and Synthetic Biology. The individual in this position...
Assistant/Associate Project Scientist - Cannabis Research. The Department of Environmental Science, Policy, and Management at the University of California, Berkeley seeks applications for an Assistant/Associate Project Scientist in the Grantham Lab, in the area of cannabis research. At least four ye...
Under the general direction of the IGI Plant Genomics and Transformation Facility (PGTF) Director, the Staff Research Associate (SRA) II is responsible for establishing and improving plant transformation and gene editing protocols in major crop species. The University of California, Berkeley, is one...
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...
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...