Clinical Research Coordinator

Job DescriptionClinical Research Coordinator IIThe Clinical Research Coordinator II will be responsible for ensuring the successful execution of clinical trials at assigned investigative sites. This role will involve ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines, as well as providing high-quality data to sponsors.Key...

Job DescriptionJob DescriptionClinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...

Job DescriptionJob DescriptionClinical Research Coordinator IThe CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study enrollment meets or exceeds...

Job DescriptionJob DescriptionClinical Research Coordinator I - PRN (As Needed/Part-time position)The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...

Job DescriptionJob DescriptionUnblinded Clinical Research Coordinator IDM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.Duties & Responsibilities:Compound and dispense prescribed IP.    ...

Job DescriptionJob DescriptionClinical Training Coordinator II (Travel)The CTC II or (CRC II) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CTCII is responsible for developing and...

Job OverviewPosition Summary:A Study Manager plays a crucial role in ensuring that high-quality research is executed at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. The objective is to deliver the highest quality data to the sponsor while meeting or exceeding enrollment expectations and achieving...

Job OverviewThe Clinical Training Coordinator II (Travel) is responsible for ensuring that high-quality research is conducted at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This role is pivotal in delivering superior quality data to sponsors and enhancing the performance and skills of site staff...

Job OverviewThe Clinical Training Coordinator II (Travel) is pivotal in ensuring that high-quality research is executed at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This role is dedicated to enhancing the performance and skills of the research staff through effective training programs....

Job OverviewThe Clinical Training Coordinator II (Travel) plays a crucial role in ensuring that high-quality research is conducted at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This position is essential for delivering superior quality data to sponsors and enhancing the performance and skills of...

Company DescriptionMIND Neurology Clinic, based in West Houston, Texas, is a neurology practice that specializes in treating a variety of neurological disorders. Role DescriptionThis is a part-time on-site role for a Clinical Research Coordinator located in Houston, TX. The Clinical Research Coordinator will be responsible for tasks related to informed...

Job DescriptionJob DescriptionResearch Assistant I The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIESCompleting DMCR-required training, including GCP and IATA.Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational...

Job DescriptionJob DescriptionResearch Assistant I The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIESCompleting DMCR-required training, including GCP and IATA.Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational...

Job DescriptionJob DescriptionResearch Assistant I The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIESCompleting DMCR-required training, including GCP and IATA.Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational...

Job DescriptionJob DescriptionResearch Assistant I- PRN (As Needed/Part-time position) The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIESCompleting DMCR-required training, including GCP and IATA.Maintaining a working knowledge of current FDA regulations,...

Job DescriptionJob DescriptionPBMC Lab Coordinator A PBMC Lab Coordinator will be primarily responsible to travel to new sites to set up Research and PBMC labs, train the new staff in addition to maintaining existing PBMC and research labs and training existing staff. Set up, provide oversight and training for special laboratory procedures for clinical...

Position OverviewAt Houston Methodist, the Clinical Research Coordinator role is pivotal in assisting various initiatives under the guidance of the Clinical Trial Manager. This includes the management of clinical research protocols, collection of patient data as outlined in study protocols, and preparation of study reports.This role is essential in ensuring...

OVERVIEWThe University of Texas M. D. Anderson Cancer Center is dedicated to the mission of eradicating cancer through exceptional programs that merge patient care, research, and prevention, alongside educational initiatives for students, professionals, and the community.POSITION SUMMARYThe primary role of the Clinical Research Coordinator is to oversee the...

At Houston Methodist, the Clinical Research Coordinator role is pivotal in assisting various projects under the guidance of the Clinical Trial Manager. This includes the implementation of clinical research protocols, collecting patient data as outlined in the study protocol, and compiling study reports. This position is essential in ensuring precise data...

About the RoleWe are seeking a highly skilled and detail-oriented Clinical Research Assistant to join our team at Evolution Research Group. As a Clinical Research Assistant, you will play a critical role in the conduct of clinical trials, ensuring the highest level of quality and compliance with regulatory requirements.Key ResponsibilitiesSubject Care and...