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. Clinical Research Coordinator I - Obstetrics & Gynecol...
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. Clinical Research Coordinator I - Obstetrics & Gynecol...
Nursing, Biology, Public Health)Minimum of 1 year of experience in clinical researchKnowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processesExperience with electronic medical records (EMR) systems is a plusCertification in clinical research (e. A company is looking for a Clinica...
Prescreening, Query Resolution.Source Document Storage/Uploads.Minimum Education and Experience Qualification Requirements: .Monday through Friday business hours.Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances).Health Benefits / Dental / Vision (Med...
A company is looking for a Clinical Research Finance Coordinator II (Pre-Award) to manage financial aspects of clinical research studies during the pre-award phase. ...
Looking for a strong Clinical Research Coordinator with 3+ years of experience for a. ...
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. Clinical Research Coordinator I - Obstetrics & Gyn...
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. Clinical Research Coordinator I - Obstetrics & Gyn...
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. The Clinical Research Coordinator will plan, develop and implement start-up procedures for multiple phase I-III research studies in a...
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants. ...
Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent Clinical research certification through SOCRA for ACRP. Under supervision, the Clinical Research Coordinator will be assigned to assist with multiple clinical research studies involving hum...
Under supervision from Principal Investigator and Clinical Research Supervisor II in the Pulmonary, Critical Care & Sleep Medicine Division, the Research Coordinator supports the ICU clinical research efforts for a variety of research projects and clinical trials focusing primarily on pulmonary diso...
The Clinical Research Coordinator (CRC-RN) serves as the lead clinical study coordinator on research protocols. Functions as a role model at the expert level of clinical and research practice, characterized by viewing situations as a whole, advanced clinical skills, teaching/mentoring of peers and d...
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 comp...
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 ...
The incumbent will work as an Assistant Clinical Research Coordinator to be responsible for coordinating and managing a clinical trial conducted by the Pacific Treatment and Research Center (Pac-TARC) at UC San Diego. Experience performing clinical research duties in a clinical research environment....
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 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 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 ...
Other responsibilities include recruiting, retaining, motivating and educating research patients in clinical trials, training other research personnel in research procedures, oversees research finances and tracking patient enrollment. The Clinical Research Coordinator will join the team at the Shile...
Under supervision from Principal Investigator and Clinical Research Supervisor II in the Pulmonary, Critical Care & Sleep Medicine Division, the Research Coordinator supports the ICU clinical research efforts for a variety of research projects and clinical trials focusing primarily on pulmonary diso...
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...
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...