48 clinical research coordinator jobs found in Los Angeles, CA

Description The Clinical Research Coordinator (CRC) contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. The CRC recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The CRC is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The CRC collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate...

Description The Clinical Research Coordinator will contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. You will have responsibility for: * The implementation of research activities for one or more studies. * Recognizing and performing necessary tasks to manage projects and prioritizes work to meet necessary deadlines. * Planning and organizing necessary tasks to ensure adherence to the study protocol and applicable Regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). * Collaborating with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Pay...

Description As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Westwood Translational Clinical Team Manager. You will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner. This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities may include: • Regulatory compliance • Patient recruitment and enrollment • Data collection • Research chart documentation • Quality assurance • Report preparation • Protocol information dissemination • Sample management • Budget reviews You will also meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development. Travel to other locations may be required. Salary Range: $80,304.48 -...

Description As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Westwood Translational Clinical Team Manager. You will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner. This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities may include: • Regulatory compliance • Patient recruitment and enrollment • Data collection • Research chart documentation • Quality assurance • Report preparation • Protocol information dissemination • Sample management • Budget reviews You will also meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development. Travel to other locations may be required. Salary Range: $80,304.48 -...

Description As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Westwood Translational Clinical Team Manager. You will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner. This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities may include: • Regulatory compliance • Patient recruitment and enrollment • Data collection • Research chart documentation • Quality assurance • Report preparation • Protocol information dissemination • Sample management • Budget reviews You will also meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development. Travel to other locations may be required. Salary Range: $80,304.48 -...

Description The Department of Medicine is actively seeking to hire a Clinical Research Coordinator, a vital position that plays a crucial role in overseeing the entire spectrum of clinical research, trials, and study activities. As a Clinical Research Coordinator, you will support the overall operational management of clinical research, study activities from design, set up, conduct, through closeout In this role, you will be responsible for managing and executing research activities across one or more studies. Your role encompasses recognizing and executing essential tasks to effectively handle projects and ensuring that work is prioritized to meet critical deadlines. As the Clinical Research Coordinator, you will oversee planning and organization of task in effort to ensure strict adherence to the study protocol and relevant regulations. This includes compliance with institutional policies and procedures, FDA Code of Federal Regulations (CFR), and the International Conference...

Description The Department of Molecular and Medical Pharmacology is seeking a detailed and dynamic Clinical Research Coordinator. In this role, you will coordinate research studies, identify participants, and assist the Principal Investigator (PI) with patient eligibility. Responsibilities also include facilitating the informed consent process, educating participants about protocol requirements, and emphasizing the significance of protocol compliance. The role requires maintaining all necessary documentation in accordance with FDA regulations, Good Clinical Practice (GCP) guidelines, and the funding source. This includes managing patient registration, data, and treatment assignment. This role will involve quality control and assurance activities related to study workflows and documentation. In addition, the Clinical Research Coordinator is responsible for procuring and distributing study supplies, including coordinating specimen collection and shipping. Ensuring the safe and...

Description The Department of Urology, Interventional Clinical Trials Unit is seeking to hire a full time Clinical Research Coordinator who will work with the PI, Sub-Investigators, research personnel and hospital staff (collectively, the Study Team) to serve as Study Coordinator and Data Manager for research studies by assuring compliance with all aspects of individual studies. You will be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). All relevant regulatory and Good Clinical Practice (GCP) guidelines must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. Further, this position requires that the individual participate in patient recruitment and enrollment, data collection,...

Description The Clinical Research Coordinator (CRC) contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. The CRC recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The CRC is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial...

Description the Department of Urology is seeking to hire a full time Clinical Research Coordinator who will contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. You will be responsible for: * The implementation of research activities for one or more studies. * Recognizing and performing necessary tasks to manage projects and prioritizes work to meet necessary deadlines. * Planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). * Collaborating with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial...

Description The David Geffen School of Medicine, Department of Surgery, Division of Liver and Pancreatic Transplant, is seeking to hire a full time Clinical Research Coordinator to function as the Study Coordinator. Under the direction of the Principal Investigator and the Clinical Trials Director, you will complete the following duties: * Research personnel and hospital staff (collectively, the Study Team) to serve as Study Coordinator and Data Manager for research studies by assuring compliance with all aspects of individual studies. * Be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). * Be responsible for adherence of all relevant regulatory and Good Clinical Practice (GCP) guidelines. * Ensuring the timely coordination and completion of study related procedures...

Description The Department of Molecular & Medical Pharmacology is seeking a skilled Clinical Research Coordinator to join our team. In this role, you will play a pivotal part in coordinating research studies and ensuring adherence to regulatory guidelines. Your responsibilities will include identifying and enrolling participants based on the approved recruitment plan, assisting the Principal Investigator (PI) in determining patient eligibility, and facilitating the informed consent process. As a Clinical Research Coordinator, your key responsibilities will involve coordinating research studies and maintaining compliance with FDA Code of Federal Regulations (CFR), Good Clinical Practice (GCP) Guidelines, and funding source requirements. You will effectively communicate protocol requirements and provide participant education on protocol compliance and the significance of their involvement. Additionally, you will manage patient registration, data, and treatment assignment,...

Description Under the supervision of the Clinical Research Center Administrator, you will provide support for the Department of Ophthalmology Clinical Research Center by managing the daily aspects of clinical trials, with a primary focus on research imaging studies and other ophthalmic studies. As a Clinical Research Coordinator, you will be the back-bone of every research project while working closely with the Principal Investigator to ensure necessary milestones are met and enforce patient safety. Responsibilities include: * Screen potential patients for protocol eligibility, present non-medical trial details, and facilitate informed consent. * Collaboratively plan and coordinate strategies for increasing patient enrollment, workflow improvements, and personnel trainings. * Facilitate communications with key stakeholders such as internal ancillaries, sponsors, principal investigators, and research teams. * Ensure compliance with all federal and local agencies...

Description The Clinical Research Coordinator will participate in all research activities as part of the clinical research team located at UCLA Westwood/UCLA Santa Monica while under the direction of the Administrative Staff Manager, the study investigators, Medical Director/ Principal Investigators in the Department of Pediatrics. You will be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner for all assigned research studies. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). All relevant regulatory and Good Clinical Practice (GCP) guidelines must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. Further, this position requires that the individual participate in patient recruitment and enrollment, data collection, source...

Description To support Clinical Trials, The Department of OBGYN is seeking to hire a full time Clinical Research Coordinator. You will work with the PI, Sub-Investigators, research personnel and hospital staff (collectively, the Study Team) to serve as Study Coordinator and Data Manager for research studies by assuring compliance with all aspects of individual studies. You will be responsible for: * Ensuring that protocol procedures have been completed accurately, safely, and in a timely manner; including the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). * Responsible for all relevant regulatory and Good Clinical Practice (GCP) guidelines which must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. * Participation in patient recruitment and enrollment, data collection, source documentation, quality...

Description The Department of OBGYN is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. You will perform necessary tasks to manage projects and prioritizes work ensuring deadlines are met. You will also be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies. This includes but is...

Description Working in the Retina Division of the Department of Ophthalmology, you will be the Clinical Research Coordinator and liaison for patients and research subjects, and provide administrative and clinical support to the Principal Investigators. Responsibilities include coordinating the daily aspects of clinical trials; schedule patients in the UCLA HIS system and CRC windows program; prepare documents for submission to the Office for Protection of Research Subjects; provide information to patients and their families with decisions on whether or not to participate in clinical research trials; take eye pressure with tonopen and dilate patient’s eyes for study purposes; data collection and preparation for research protocols; take patient history and assist during clinical examinations; assist faculty and staff with obtaining proper data at the time of patient visits; provide input for budget submissions to Office of Contracts and Grants; assist physicians in the...

Description The mission of the Coordination Services and Education (CSE) unit in the CTSI's Office of Clinical Research (OCR) is to provide a sales and service solution to investigators and study teams seeking assistance with clinical research study start up, on-study coordinator study and patient management, regulatory maintenance, data entry services and clinical research training and education through three dedicated teams: Study Activation Team, Clinical Research Coordinator Team and the Education and Training Team. Each Clinical Research Coordinator (CRC) supports multiple clinical research studies ensuring adherence to federal/local/institutional regulatory requirements, good clinical practice, data quality, protocol compliance, protection of human subjects, and overall quality assurance and quality management. In this role, you will contribute to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through...

Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. In this role, you will perform necessary project management tasks and prioritizes work to reach scheduled goals and will be responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner. You will work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of studies. The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical...

Description Take on a critical role with a world-renowned research leader. Help advance life-changing medical breakthroughs. Take your career to a higher level. You can do all this and more at UCLA Health. You will play a key part in the operational management of clinical research/trial/study activities - from design, set up, and conduct through closeout. You will have direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials, local investigator-initiated clinical trials, and/or programmatic clinical research activities. You will ensure study protocols and procedures are completed in an accurate, safe, and timely manner. You will work with principal investigators, departments, sponsors, institutions, and other entities to support compliance, financial, personnel, and other related aspects of each study. You may also supervise and train others. Salary: $6692.04 - $10765.38/month Qualifications...