Conducts 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 moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the c...
read moreContributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues. The CRC II provides leadership and supervisio...
read moreThe Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout ...
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 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 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 (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 moreThe Clinical Research Coordinator Bilingual Mandarin/English (CRC Bilingual Mandarin/English) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not lim...
read moreAs 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 moreA Clinical Research Coordinator (CRC) I position is currently available to support our Multiple Myeloma Program within the Tisch Cancer Institute. News & World Report's "Best Children's Hospitals" ran...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the c...
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 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 moreAs 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 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 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 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 moreThe Clinical Research Coordinator Bilingual Mandarin/English (CRC Bilingual Mandarin/English) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not lim...
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 Seni...
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 moreWe are seeking a highly motivated and detail-oriented Clinical Research Data Coordinator with a primary focus on oncology research. CCRP (Certified Clinical Research Professional) or ACRP (Association...
read moreWe are seeking a highly motivated and detail-oriented Clinical Research Data Coordinator with a primary focus on oncology research. CCRP (Certified Clinical Research Professional) or ACRP (Association...
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 morePREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Reports to Director of Clinical Trials or Clinical Research Nurse ...
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 Seni...
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 Seni...
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 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). Reviews study with principal investigat...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Reviews study with principal investigat...
read moreIn research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Coordinates and monitors research trials; actively oversees the r...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the c...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the c...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the c...
read morePrimary Duties and Responsibilities:.Act as project manager on studies as directed by department manager.Assist in the conduct of clinical trials as specified by the study protocol under the supervisi...
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...
read moreMinimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory complian...
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