As a Research Coordinator, you will be an integral member of our research team, and support the conduct of an NIH-funded randomized trial to investigate the effects of an information-sharing intervent...
read moreAssist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.
The 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 coordinates and assists with the daily operations of clinical research studies. The Coordinator drives recruitment and assists research participants on clinical resea...
read moreThe Addiction Institute of Mount Sinai is looking for a Clinical Research Coordinator I that assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains...
read moreThe Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials. The Clinical Research Coordinator acts as a liaison between princi...
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 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 moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal inv...
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 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 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 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 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 moreAssociation of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred...
read moreAssociation of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred...
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 assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
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 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 moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...
read moreThe Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts...
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...
read moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
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 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). In collaboration with the principal inv...
read moreIn research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Adheres to good clinical practice, and complies with regulatory a...
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 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 moreIn research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Adheres to good clinical practice, and complies with regulatory a...
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...
read morePosition Summary The Clinical Research Coordinator (CRC) will provide support for research activities in the Division of Nephrology. Responsibilities Obtain informed consent Organize and conduct basel...
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