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...
A company is looking for an Industry Research Agreements Coordinator responsible for managing sponsored project agreements funded by industry partners. ...
Under the supervision of the PI, the incumbent is responsible for coordinating all clinical research aspects of research projects involving human subjects, from initiation through completion. Or Bachelor's degree from an accredited college/university in clinical research administration, health scien...
A non-profit organization is looking for a Research Coordinator. ...
The CFCCC provides research resources to its ~175 members engaged in research and offers multidisciplinary cancer care to its patients. Supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing comprehensive data management for a research portfolio of Phase I...
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...
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. ...
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. Organize and l...
Overseeing the smooth execution of internal research studies, including scheduling, recruitment, patient consent, and administering questionnaires. Manage IRB submissions and study progress for internal and external research studies and ensure that documentation and requirements are up to date. Appr...
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. Minimum 2 years of research experience (5 is ideal). Coordinate and maintain diverse activ...
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...
Under the direction of the Program Manager, the Assistant Clinical Research Coordinator supports the research efforts of several regional projects. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. The mission of...
The Research Nurse Coordinator (RNC) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians. The RNC provides support, coordination and leadership for FDA regulated research including drug/device/biologic studies that may involve industry ...
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...
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. Communicate effectively with study participants, investigators, and ...
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...
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). Incumbent is responsible for all aspects of clinical research from initiation through co...
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...
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...
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. Minimum 2 years of research experience (5 is ideal). Coordinate and maintain diverse activ...
The Clinical Research Regulatory Coordinator will support clinical research teams (physicians, nurses, etc. Will be responsible for ensuring that all research studies are compliant with regulations as well as maintain accurate and up-to-date regulatory files. Will serve as a central resource for sta...
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...