Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Oversee execution of protocols to...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. The Department of Neurosciences a...
read moreExperience performing clinical research duties in a clinical setting (e. Under supervision, the Clinical Research Coordinator Assistant will assist with study start-up, recruitment, data collection, c...
read moreDemonstrated 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...
read moreUnder supervision, the Clinical Research Coordinator Assistant will assist with study start-up, recruitment, data collection, compliance, and administrative support for multiple Phase I-III clinical t...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Strong experience in clinical tri...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Translational research is carried...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Translational research is carried...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Translational research is carried...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Translational research is carried...
read moreOur core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS program...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. The Department of Neurosciences a...
read moreOur core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS program...
read moreOur core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS program...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreOur core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS program...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreOur core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS program...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreDemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. The Department of Neurosciences a...
read moreUnder the supervision of the Site Director, the Clinical Research Coordinator I is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is ma...
read moreUnder the supervision of the Site Director, the Clinical Research Coordinator I is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is ma...
read moreProfound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. The Clinical Research Coordinator wil...
read moreProfound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. The Clinical Research Coordinator wil...
read moreWorks collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation...
read moreTwo years' experience in a clinical research setting (preferred), working as a coordinator on Industry-Sponsored clinical trials. Works collaboratively with the other members of the clinical research ...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreA BA/BS in biological sciences, public health, or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of clinical trials research experience, including two year...
read moreConducts and coordinates tasks involved with the execution of the in-house clinical research projects in accordance with the clinical protocol, Clinical Affairs Donation Center SOPs/WIs, GCP guideline...
read moreConducts and coordinates tasks involved with the execution of the in-house clinical research projects in accordance with the clinical protocol, Clinical Affairs Donation Center SOPs/WIs, GCP guideline...
read moreThe Clinical Research Coordinator I supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. Al...
read moreThe Clinical Research Coordinator I supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. Al...
read moreThe Clinical Research Coordinator will collaboratively work with the Principal Investigators (PI), sub-investigators, clinical, and ancillary departments to assist with research studies. Additionally,...
read moreCertified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent Clinical research certification through SOCRA for ACRP. Under supervision, the Clinical R...
read moreCertified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent Clinical research certification through SOCRA for ACRP. Under supervision, the Clinical R...
read moreUnder 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...
read moreThe Assistant Clinical Research Coordinator is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including creating study specific sourc...
read moreThe Assistant Clinical Research Coordinator is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including creating study specific sourc...
read moreDuties include but not limited to: interpreting research protocols; recruiting subjects; screening for eligibility including obtaining vital signs, ECGs, height and weight; monitoring and timely repor...
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