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). Incumbent is responsible for all aspects of clinical research from initiation through completion of research p...
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 Social Impact Hub, which fosters innovative research, community engagement, and policy development for social change, seeks a dynamic and motivated individual with experience in event coordination, research, policy, communications, and program administration. Additionally, the coordinator will i...
The Social Impact Hub, which fosters innovative research, community engagement, and policy development for social change, seeks a dynamic and motivated individual with experience in event coordination, research, policy, communications, and program administration. Additionally, the coordinator will i...
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 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). S/he will work with the clinical research team to manage and collect accurat...
The coordinator is also responsible for managing payment confirmations, responding to sponsor requests and researching patient visits in the Electronic Medical Records (EMR) system to facilitate reimbursement. The Financial Coordinator plays a key support role, assisting with various financial respo...
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). Incumbent is responsible for all aspects of clinical research from initiation through completion of research p...
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. ...
The Clinical Research Assistant (CRC) works collaboratively with Principal Investigators (PI) sub-investigators, clinical and ancillary departments, to assist with research studies in subject recruitment, data collection, scheduling of study-related activities, and follow-up of enrolled subjects. 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 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...
We are seeking a dedicated and motivated Clinical Research Coordinator with a strong background in community outreach activities, particularly within the Asian community, with a focus on the Filipino community. This role is vital in bridging the gap between our clinical research initiatives and the ...
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 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 ...
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. ...
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 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...
Under the direction of the Manager of Development Operations, this position supports the Development Department in which principal responsibilities include researching, analyzing and providing high-level research on high-net-wealth individuals, corporations and foundations using a variety of biograp...