The 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 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 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 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 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 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 moreIndividual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine. We have an exciting opportunity to join...
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 (CRC) will work under the direct supervision of the Clinical Research Manager. As an integral member of the clinical research team, the Clinical Research Coordinator ...
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 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 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 (CRC) will work under the direct supervision of the Clinical Research Manager. As an integral member of the clinical research team, the Clinical Research Coordinator ...
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 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 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 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’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...
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 Princip...
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 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 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 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 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 moreClinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical...
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 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 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 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 Laboratory Coordinator plays a crucial role in the execution of clinical lab testing protocols, and new assay and new instruments validation and verification. The coordinator will help to perform ...
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 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...
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