Clinical Research Data Spec I

GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...

Opening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...

Opening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...

GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...

Opening Full Time 40 hours Range URG 106 Surgery-Cancer Control Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree...

GENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability to exercise some independent judgment, flexibility to vary specific tasks as...

GENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability to exercise some independent judgment, flexibility to vary specific tasks as...

Opening Full Time 40 hours Range URG 106 Surgery-Cancer Control Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree...

Human Subject Research Spec I Next Job Apply for Job When you are ready to apply, registering only takes a minute. Your online account allows you to upload your resume or CV, apply for jobs and access our online career tools. For general questions ab Research, Technology, Education

This is a full-time position (40 hrs/wk) in Ob/ Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the Principal I Clinical Research, Research, Data Entry, Research Coordinator, Operations, Technology, Education

This is a full-time position (40 hrs/wk) in Ob/ Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the Principal I Clinical Research, Research, Data Entry, Research Coordinator, Operations, Technology, Education

Human Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with human subject research. They will work under the supervision and guidance of the Principal Investigator (P Clinical Research, Research Coordinator, Research, Technology, Clinical

Human Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with human subject research. They will work under the supervision and guidance of the Principal Investigator (P Clinical Research, Research Coordinator, Research, Technology, Clinical

The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education

The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education

Opening Full Time 40 hours Range URG 108 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project...

GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...

GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...

Opening Full Time 40 hours Range URG 108 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project...

Opening Full Time 40 hours Range URG 106 Ortho, Clinical Research Schedule 8 AM-4:30 PM; OCC WKNDS Responsibilities GENERAL PURPOSE: Coordinates the activities associated with human subject research. This person will be responsible for recruitment and have administrative responsibilities, including screening and recruiting subjects, performing informed...