The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.   KEY RESPONSIBILITIES: - Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. - Assists with patient recruitment. -

KEY RESPONSIBILITIES: - Recruits, orients, and supervises research administration staff or independently manages the most complex research administration activities associated with the conduct of clinical trials. - Manages a large or multiple smaller clinical research projects. - Manages clinical trials related information systems. -

KEY RESPONSIBILITIES: - Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects. - Trains and provides guidance to less experienced staff. - Oversees data management for research projects. - Interfaces with research participants and resolves...

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.   KEY RESPONSIBILITIES: - Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. - Assists with patient recruitment. -

KEY RESPONSIBILITIES: - Functions as the principal investigator, co-principal investigator, or project director of sponsored projects. - Has primary authority over the conduct of a project including protocol development and adherence, human subjects, personnel management and budget oversight. - Publishes study results as first author or co-author. -

Are you passionate about making a difference in the health and well-being of African-American women? We’re looking for a dedicated and detail-oriented Clinical Research Coordinator I to join our team in a dynamic and impactful role. As part of our research team, you’ll play a key role in advancing our understanding of heart and sleep health among African-American women. You’ll be responsible for recruiting and scheduling research participants, conducting onsite visits, and collecting valuable data that will drive important health discoveries....

The School of Nursing is searching for a Senior Research Interviewer. This position will be responsible for study participant screening and recruitment, medical record reviews, survey administration, semi-structured qualitative interviews, and data entry and verification.   KEY RESPONSIBILITIES: - Recruits, screens, identifies, contacts, and interviews participants to obtain data for assigned research projects. -

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials.    KEY RESPONSIBILITIES: - Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms. - Provides guidance to less experienced staff. -

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.   KEY RESPONSIBILITIES: - Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. - Assists with patient recruitment. -

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.   KEY RESPONSIBILITIES: - Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. - Assists with patient recruitment. -

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials.    KEY RESPONSIBILITIES: - Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms. - Provides guidance to less experienced staff. -

KEY RESPONSIBILITIES: - Functions as the principal investigator, co-principal investigator, or project director of sponsored projects. - Has primary authority over the conduct of a project including protocol development and adherence, human subjects, personnel management and budget oversight. - Publishes study results as first author or co-author. -

Experience with clinical research interviewing (particularly with psychiatric populations), statistical packages, experiment software (Eprime or other), electroencephalography, physiology recording and/or neuroimaging data collection and/or processing preferred. Educational background in neuroscience or psychology is also preferred, but not required. Assist with the training of incoming lab members on study procedures. Must be highly detail oriented, organized, and able to flexibly move between different tasks. Must be able to work effectively with interdisciplinary team members at different stages of training.    

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.   KEY RESPONSIBILITIES: - Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. - Assists with patient recruitment. -

KEY RESPONSIBILITIES: - Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects. - Trains and provides guidance to less experienced staff. - Oversees data management for research projects. - Interfaces with research participants and resolves...

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials.    KEY RESPONSIBILITIES: - Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms. - Provides guidance to less experienced staff. -

KEY RESPONSIBILITIES: - Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects. - Trains and provides guidance to less experienced staff. - Oversees data management for research projects. - Interfaces with research participants and resolves...

KEY RESPONSIBILITIES: - Responsible for directing and managing large and highly complex clinical research groups. - With support from operational leadership, assesses team performance, manages distribution of staff workload, and ensures compliance amongst staff. - Supervises staff to include performance management and development, recruitment, on-boarding. -

JOB DESCRIPTION: - Responsible for directing and managing large and highly complex clinical research groups. - With support from operational leadership, assesses team performance, manages distribution of staff workload, and ensures compliance amongst staff. Supervises staff to include performance management and development, recruitment, on-boarding. - May serve as a back-up and fill temporary portfolio management needs. -

JOB DESCRIPTION: - Responsible for directing and managing large and highly complex clinical research groups. - With support from operational leadership, assesses team performance, manages distribution of staff workload, and ensures compliance amongst staff. Supervises staff to include performance management and development, recruitment, on-boarding. - May serve as a back-up and fill temporary portfolio management needs. -