The Clinical Research Coordinator is an active participant in the coordination of cancer related clinical research studies from research planning to completion of studies. The Clinical Research Coordi...
read moreIndividual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine. Contributes to the preparation of artic...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreObtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies ...
read moreMinimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...
read moreA Clinical Research Coordinator II position is currently available within the Medicine Clinical Trials Office. Under the supervision of the clinical research manager, the coordinator maintains procedu...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreIndividual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine. Contributes to the preparation of artic...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreAt least two (2) years' experience in research and study related activities. Under general supervision with latitude for independent judgment and initiative, assists in the planning, organizing and co...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreThis includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, p...
read moreThe Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreThis includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, p...
read moreThe Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreResponsible for coordinating and performing study specific clinical activities across multiple study protocols of different pediatric therapeutic areas and phases, in accordance with appropriate regul...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreThe Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits, and serves as principal administrative liaison f...
read moreThe Clinical Research Coordinator coordinates and assists with the daily operations of clinical research studies. The Coordinator drives recruitment and assists research participants on clinical resea...
read moreThis position is for a full-time Clinical Research Coordinator I (CS02) in the Eating and Weight Disorders Program. This position requires a candidate with a master's degree, trained in psychotherapy ...
read moreConducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the PI and ...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreTrains clinical staff on study protocols and procedures and supervises the Clinical Research Unit (CRU) staff when the principal investigator or sub-investigators are not present to direct clinical re...
read moreExperience working with clinical research studies and clinical trials, preferred. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; mai...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Clin...
read moreExperience working with clinical research studies and clinical trials, preferred. Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good cli...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Clin...
read moreMinimum of 1 year experience as a Clinical Research Coordinator. We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our team in Livingston, NJ. Maintain comprehensive...
read morePerform department specific procedures as qualified by training and evaluation of proficiency (clinical study evaluations and measurements). Eurofins is the global leader in food, environment, pharmac...
read moreMinimum of three years in a Study Coordinator or Clinical Research Coordinator role. Oncology Clinical Research Coordinator. This is a contract position and requires previous Oncology clinical researc...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...
read moreThe Clinical Research Coordinator I will be the point person for multiple research projects and help establish, track, oversee, and monitor neuroimaging acquisition protocols, data transfer, and data ...
read moreThe Clinical Research Coordinator I will be the point person for multiple research projects and help establish, track, oversee, and monitor neuroimaging acquisition protocols, data transfer, and data ...
read moreThe Clinical Research Coordinator is an active participant in the coordination of critical care and resuscitation research studies from research planning to completion of studies. The Clinical Researc...
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