This includes a diverse portfolio of research trials involving multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials and any subsites, and programmatic clinical research activities such as a clinical database and biorepositories, NIH and FDA repo...
Experience performing clinical research duties in a clinical research environment. Experience performing clinical research duties in a clinical research environment. Assistant Clinical Research Coordinator - 130344. Responsible for coordinating and managing clinical trials including providing all as...
The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI). Experience in clinical research or demonstrated research or training experience that translates int...
This position is to serve as the Clinical Research Coordinator for a series of cross-discipline projects within the School of Medicine (SOM) Divisions of Biomedical Sciences and Clinical Sciences, with primarily focus on clinical trials sponsored by the California Institute for Regenerative Medicine...
Assistant Clinical Research Coordinator (Neuro-Spine). Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepar...
Key Responsibilities:Collaborate with research staff to identify, recruit, and enroll eligible patients for clinical trials virtuallyCollect, maintain, and store all relevant data associated with clinical research trialsInteract with potential participants to educate them regarding clinical research...
The Clinical Research Coordinator II is crucial to the companies clinical research, managing multiple complex trials across various areas and phases. An exciting Clinical Site Network are looking to bring on board a Clinical Research Coordinator to either of their sites based out of. Minimum of 3+ y...
The Clinical Research Coordinator will be responsible for running clinical research studies under the supervision of the PI. The role will include training on clinical trial protocols, recruitment of patients, conduct informed consent with subjects, conduct screening and follow up visits, data entry...
The Clinical Research Coordinator will plan, direct, or coordinate clinical research projects, and will evaluate and analyze clinical data. Works with PI, co-investigators and trainees on the research team to facilitate completion of research proposals, projects, manuscripts, abstracts and presentat...
The Clinical Research Coordinator Supervisor (CRC-Su) functions independently and is responsible for the complete coordination of multiple assigned human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Cl...
The Clinical Research Coordinator will plan, direct, or coordinate clinical research projects, and will evaluate and analyze clinical data. Works with PI, co-investigators and trainees on the research team to facilitate completion of research proposals, projects, manuscripts, abstracts and presentat...
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 Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal Investigator (PI), assists in the operational and administrative research support of the Kaiser Permanente Northern California (KPNC) PI and KPNC Clinical Trials Operati...
The Clinical Research Coordinator Assistant (CRC-A), in conjunction with Clinical Research Coordinators, assists in the coordination of details of human subjects’ (clinical) research and documentation concerning study protocols. The CRC-A is the entry position in the Clinical Research Coordinator se...
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 ...
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance for journey-level work at the next level within the s...
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 Clinical Research Coordinator (CRC) will ensure successful implementation of and adherence to clinical research protocols regarding planning, administration, timeline management enrollment, participant engagement data collection and reporting. Study duties include the coordination of research pr...
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 Clinical Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal Investigator (PI), assists in the operational and administrative research support of the Kaiser Permanente Northern California (KPNC) PI and KPNC Clinical Trials Operati...