Sr Clinical Research Spec

We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for older adults with cancer. The Senior Research Coordinator will play a pivotal role in the execution Clinical Research, Clinical, Research, Clinic, Research Coordinator, Diversity, Healthcare, Education

Sr Safety and Comp Spec, Facil 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 a Safety, Manufacturing, Education

The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ul Clinical Research, Clinical, Research, Research Coordinator, Monitoring, Operations, Healthcare

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

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...

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...

Responsibilities **Job Summary:** 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 of staff, providing both clinical and administrative supervisory support...

Responsibilities **Job Summary:** 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 of staff, providing both clinical and administrative supervisory support...

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

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

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....

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