Clinical Trials Proj Spec I A

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 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...

With direction from the Clinical Research Manager, assists with coordination of clinical research management activities for large international multi-site studies within the Clinical Cardiology Research Center to be consistent with Good Clinical Prac Clinical, Clinical Research, Healthcare, Media, Training, Electronic

The Clinical Research Project Manager (CRPM) position involves working with multiple principal investigators across multiple clinical trials with a wide variety of assessment methods including patient-reported, biological, physiological, and electron Clinical, Clinical Research, Project Management, Equipment, Auditor, Exercise, Education

The Clinical Project Lead directs and coordinates all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment and acts as a liaison to study leadership and sponsor(s). Individual ensures st Clinical, Clinical Research, Project Management, Project Coordinator, Project Lead, Lead, Business Services

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 proced Clinical Research, Clinical, Research, Data, Monitoring, Management, Technology

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 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...

This position requires working with cancer patients and survivors at Wilmot Cancer Institute locations by managing all research activities for Re. NEW within the PEAK Human Performance Science Program; a clinical and implementation exercise oncology Clinical, Clinical Research, Exercise, Healthcare, Education, Development, Oncology, Patient

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

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...

The Med Technologist-Spec is responsible for the timely and accurate reporting of results, maintenance and troubleshooting of laboratory instrumentation, development of new procedures and instruments, writing/updating of procedure manuals, training o Med Tech, Technologist, Clinical, Chemistry, Laboratory, Technical, Healthcare

This position is available only to those currently in a Contractor position in the Clinical Mass Spec Lab Performs analyses on blood, tissue, and body fluids to aid health care providers in the diagnosis, prognosis, and treatment of patients. Participates in the operational support activities necessary to maintain and optimize testing capabilities....