Registered Nurse (RN), Research Coordinator, Radiation Oncology
Posted on Sep 28, 2024 by University of Maryland Medical System
Upper Marlboro, MD
Health Care
Immediate Start
Annual Salary
Full-Time
Job Description
Under general supervision, coordinates the implementation of research protocols approved for activation at the University of Maryland Medical System. Participates in complex clinical trial; ability; ability to work independently. Acts as a resource to the Research Nurse Coordinators.
Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
Participates in, supervises and conducts complex clinical research studies.Screens patients for eligibility to enter research studies. Ensures that diagnostic tests required for entry to a study are ordered and performed. Assists physicians and/or principal investigators in obtaining informed consent.
Conducts patient/family education concerning clinical studies.
Administers investigational drugs as required by treatment protocols.
Follows the clinical course of patients entered on clinical research studies by obtaining results of diagnostic studies, assessing patients for complications, and recording patient data onto study forms.
Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines
Records pertinent patient information on flow sheets and other case report forms and delegates these tasks to data management staff when appropriate.
Acts as liaison between the institution and the study sponsor by preparing study reports and communicating with clinical study monitors.
Maintains clinical database(s) on patients participating in clinical studies and/or seen by a specific clinical service and oversees data entry by data management staff.
Assists clinical investigator with study initiation, conduction, and completion.Communicates with the Institutional Review Board (IRB) and other departmental review committees.
Confirms appropriateness of drug doses in accordance with protocols.
Acts as a consultant to members of the health care team.
Educates faculty and hospital staff by providing written and oral presentations related to protocol treatment administration and procedures.
Communicates treatment modifications and amendments to faculty and staff.
Prepares study results for presentation and/or publication.
Prepares and responds to audits conducted by study sponsors.
Acts as a resource for the Research Nurse Coordinators.
Represents department at research and protocol initiation meetings.
Under general supervision, coordinates the implementation of research protocols approved for activation at the University of Maryland Medical System. Participates in complex clinical trial; ability; ability to work independently. Acts as a resource to the Research Nurse Coordinators.
Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
Participates in, supervises and conducts complex clinical research studies.Screens patients for eligibility to enter research studies. Ensures that diagnostic tests required for entry to a study are ordered and performed. Assists physicians and/or principal investigators in obtaining informed consent.
Conducts patient/family education concerning clinical studies.
Administers investigational drugs as required by treatment protocols.
Follows the clinical course of patients entered on clinical research studies by obtaining results of diagnostic studies, assessing patients for complications, and recording patient data onto study forms.
Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines
Records pertinent patient information on flow sheets and other case report forms and delegates these tasks to data management staff when appropriate.
Acts as liaison between the institution and the study sponsor by preparing study reports and communicating with clinical study monitors.
Maintains clinical database(s) on patients participating in clinical studies and/or seen by a specific clinical service and oversees data entry by data management staff.
Assists clinical investigator with study initiation, conduction, and completion.Communicates with the Institutional Review Board (IRB) and other departmental review committees.
Confirms appropriateness of drug doses in accordance with protocols.
Acts as a consultant to members of the health care team.
Educates faculty and hospital staff by providing written and oral presentations related to protocol treatment administration and procedures.
Communicates treatment modifications and amendments to faculty and staff.
Prepares study results for presentation and/or publication.
Prepares and responds to audits conducted by study sponsors.
Acts as a resource for the Research Nurse Coordinators.
Represents department at research and protocol initiation meetings.
Reference: 202631934
https://jobs.careeraddict.com/post/95633244
Registered Nurse (RN), Research Coordinator, Radiation Oncology
Posted on Sep 28, 2024 by University of Maryland Medical System
Upper Marlboro, MD
Health Care
Immediate Start
Annual Salary
Full-Time
Job Description
Under general supervision, coordinates the implementation of research protocols approved for activation at the University of Maryland Medical System. Participates in complex clinical trial; ability; ability to work independently. Acts as a resource to the Research Nurse Coordinators.
Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
Participates in, supervises and conducts complex clinical research studies.Screens patients for eligibility to enter research studies. Ensures that diagnostic tests required for entry to a study are ordered and performed. Assists physicians and/or principal investigators in obtaining informed consent.
Conducts patient/family education concerning clinical studies.
Administers investigational drugs as required by treatment protocols.
Follows the clinical course of patients entered on clinical research studies by obtaining results of diagnostic studies, assessing patients for complications, and recording patient data onto study forms.
Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines
Records pertinent patient information on flow sheets and other case report forms and delegates these tasks to data management staff when appropriate.
Acts as liaison between the institution and the study sponsor by preparing study reports and communicating with clinical study monitors.
Maintains clinical database(s) on patients participating in clinical studies and/or seen by a specific clinical service and oversees data entry by data management staff.
Assists clinical investigator with study initiation, conduction, and completion.Communicates with the Institutional Review Board (IRB) and other departmental review committees.
Confirms appropriateness of drug doses in accordance with protocols.
Acts as a consultant to members of the health care team.
Educates faculty and hospital staff by providing written and oral presentations related to protocol treatment administration and procedures.
Communicates treatment modifications and amendments to faculty and staff.
Prepares study results for presentation and/or publication.
Prepares and responds to audits conducted by study sponsors.
Acts as a resource for the Research Nurse Coordinators.
Represents department at research and protocol initiation meetings.
Under general supervision, coordinates the implementation of research protocols approved for activation at the University of Maryland Medical System. Participates in complex clinical trial; ability; ability to work independently. Acts as a resource to the Research Nurse Coordinators.
Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
Participates in, supervises and conducts complex clinical research studies.Screens patients for eligibility to enter research studies. Ensures that diagnostic tests required for entry to a study are ordered and performed. Assists physicians and/or principal investigators in obtaining informed consent.
Conducts patient/family education concerning clinical studies.
Administers investigational drugs as required by treatment protocols.
Follows the clinical course of patients entered on clinical research studies by obtaining results of diagnostic studies, assessing patients for complications, and recording patient data onto study forms.
Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines
Records pertinent patient information on flow sheets and other case report forms and delegates these tasks to data management staff when appropriate.
Acts as liaison between the institution and the study sponsor by preparing study reports and communicating with clinical study monitors.
Maintains clinical database(s) on patients participating in clinical studies and/or seen by a specific clinical service and oversees data entry by data management staff.
Assists clinical investigator with study initiation, conduction, and completion.Communicates with the Institutional Review Board (IRB) and other departmental review committees.
Confirms appropriateness of drug doses in accordance with protocols.
Acts as a consultant to members of the health care team.
Educates faculty and hospital staff by providing written and oral presentations related to protocol treatment administration and procedures.
Communicates treatment modifications and amendments to faculty and staff.
Prepares study results for presentation and/or publication.
Prepares and responds to audits conducted by study sponsors.
Acts as a resource for the Research Nurse Coordinators.
Represents department at research and protocol initiation meetings.
Reference: 202631934
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