Under the direction of the Principal Investigator and Program Manager, the Assistant Clinical Research Coordinator supports the research efforts of several research projects, including regional projects and national clinical trials with the opportunity to interface with local and national level lead...
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...
Under the direction of the Principal Investigator and Program Manager, the Clinical Research Coordinator supports the efforts of several research projects, including regional projects and national clinical trials with the opportunity to interface with local and national level leaders in medicine and...
Under the supervision of 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 wellness of people in Orange County...
Under the supervision of the Clinical Research Manager (CRM) within the Clinical Trials Unit, the Senior Clinical Research Coordinator (SCRC) supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for complicated Phase I-IV cancer prot...
We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) with at least 2 years of experience in clinical research. At least 2 years of experience as a Clinical Research Coordinator or in a similar role. Coordinate and manage clinical trials from start-up to close-out, en...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
Must have minimum 2 years experience in a clinical research setting where you actually managed patients: consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data. Coordinate the collection of biospecimens for stand-alone research projects and within cli...
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...
Under the direction of the Program Manager, the Assistant Clinical Research Coordinator supports the research efforts of several regional projects. Preferred: Master's degree and/or experience in public health or clinical research. The campus has produced five Nobel laureates and is known for its ac...
We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) with at least 2 years of experience in clinical research. At least 2 years of experience as a Clinical Research Coordinator or in a similar role. Coordinate and manage clinical trials from start-up to close-out, en...
Your Role on the Team Under the supervision of 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 wellness of p...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Maintains research practices usi...
We are seeking a Clinical Research Coordinator with a minimum of 2 years of experience in a clinical research setting. Job Title: Clinical Research Coordinator. Minimum 2 years of clinical research experience. ...
Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years experience in a Clinical Research setting. F02 AMG Clinical Trials: Required to have College Degree. Upon hire: Phlebotomy C...
Minimum of three years in a Study Coordinator or Clinical Research Coordinator role. Oncology Clinical Research Coordinator. This is a contract position and requires previous Oncology clinical research experience*. ...
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...
The candidate will help coordinate among Clinical Research Coordination team members conducting investigational clinical studies in accordance with Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. Become an expert u...
The Clinical Research Coordinator 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 each...
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical tri...
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 ...
Clinical Research Coordinators need to engage with research subjects, explain what is expected of them and understand their concerns, requiring excellent interpersonal and communicative skills. We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position...
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...
Must have minimum 2 years experience in a clinical research setting where you actually managed patients: consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data. Coordinate the collection of biospecimens for stand-alone research projects and within cli...