Clinical Research Coordinator I, SLASH

Job DescriptionThe 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 accurate and timely source documents, data collection, documentation, entry, and...

Job DescriptionThe 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 accurate and timely source documents, data collection, documentation, entry, and...

Job DescriptionThe 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 accurate and timely source documents, data collection, documentation, entry, and...

Job DescriptionCome join our team!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 accurate and timely source documents, data collection,...

Job DescriptionThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.  Evaluates and abstracts research data and ensures compliance with protocol and research objectives.  Responsible for completing case report forms, entering...

We are delighted to announce an opening for a full time Research Coordinator I to join Dr. Hussein Yassine’s research team at the University of Southern California beginning May 2024.Dr. Yassine seeking a CRC to assist with: Maintaining IRB submissions & continuing reviews, assisting with REDCap build, participant recruitment, presence at community events...

Job DescriptionThe 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 accurate and timely source documents, data collection, documentation,...

Job Description 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 accurate and timely source documents, data collection, documentation,...

Job DescriptionThe 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 accurate and timely source documents, data collection, documentation,...

We are delighted to announce an opening for a full time Research Coordinator I to join Dr. Hussein Yassine's research team at the University of Southern California beginning May 2024.Dr. Yassine seeking a CRC to assist with: Maintaining IRB submissions & continuing reviews, assisting with REDCap build, participant recruitment, presence at community events as...

Pride Health is hiring for a Clinical Research Nurse Coordinator for a client in Irvine, CA! (Contract)Schedule: Monday-Friday (8am-5pm)Contract: 6 month contractPay Rate: $53-56/hourPrimary Responsibilities:The Research Nurse Coordinator (RNC) oversees all aspects of clinical research activities.Closely collaborate with study physicians throughout the...

Job DescriptionThe Clinical Research Specialist I provides clinical research expertise by participating in the design and implementation of research projects as needed. Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership. May implement and...

Job Summary:As a Clinical Research Assistant, you will play a crucial role in supporting the execution of clinicalresearch studies and trials. Working under the supervision of the Principal Investigator or ClinicalResearch Coordinator, you will contribute to the efficient and ethical conduct of research by performingvarious tasks related to data collection,...

Job Summary:As a Clinical Research Assistant, you will play a crucial role in supporting the execution of clinicalresearch studies and trials. Working under the supervision of the Principal Investigator or ClinicalResearch Coordinator, you will contribute to the efficient and ethical conduct of research by performingvarious tasks related to data collection,...

Job Summary:As a Clinical Research Assistant, you will play a crucial role in supporting the execution of clinicalresearch studies and trials. Working under the supervision of the Principal Investigator or ClinicalResearch Coordinator, you will contribute to the efficient and ethical conduct of research by performingvarious tasks related to data collection,...

Position SummaryThe research assistant is primarily responsible for assisting in research patient visits according to ICH-GCPguidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-dayactivities may include all or some of the essential functions listed below, depending upon individualexperience / knowledge and the...

Position SummaryThe research assistant is primarily responsible for assisting in research patient visits according to ICH-GCPguidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-dayactivities may include all or some of the essential functions listed below, depending upon individualexperience / knowledge and the...

Position SummaryThe research assistant is primarily responsible for assisting in research patient visits according to ICH-GCPguidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-dayactivities may include all or some of the essential functions listed below, depending upon individualexperience / knowledge and the...

Job DescriptionWhen the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. With a team focused on effective pain management and quick recovery, Cedars-Sinai has been ranked as the No. 1 hospital...

Job DescriptionWhen the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. With a team focused on effective pain management and quick recovery, Cedars-Sinai has been ranked as the No. 1 hospital...