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UNIV - Research Nurse Manager - Hollings Cancer Center

Job in Charleston, Charleston County, South Carolina, 29408, USA
Listing for: Musckids
Full Time position
Listed on 2025-12-01
Job specializations:
  • Nursing
    Nurse Practitioner, Nurse Educator, Healthcare Nursing, RN Nurse
Job Description & How to Apply Below
UNIV - Research Nurse Manager - Hollings Cancer Center page is loaded## UNIV - Research Nurse Manager - Hollings Cancer Center locations:
Charleston time type:
Full time posted on:
Posted Yesterday job requisition :
R
- ** Job Description Summary
** The Hollings Cancer Center (HCC) Nurse Manager II is responsible for the provision of nursing education and mentorship to the non-nursing staff HCC Clinical Trials Office (CTO) and serves as a liaison to other clinical services and providers within HCC outpatient and inpatient clinics, the HCC infusion center, and other ancillary departments.
** Entity
* * Medical University of South Carolina (MUSC - Univ)
** Worker Type
** Employee
* * Worker Sub-Type
** Classified
* * Cost Center
** CC001331 HCC Administration CC
** Pay Rate Type
** Salary
* * Pay Grade
** University-08
** Pay Range
** 69,764.

- ** Scheduled Weekly Hours
** 40
* * Work Shift
**** Job Description
** The Hollings Cancer Center (HCC) Nurse Manager II is responsible for the provision of nursing education and mentorship to the non-nursing staff HCC Clinical Trials Office (CTO) and serves as a liaison to other clinical services and providers within HCC outpatient and inpatient clinics, the HCC infusion center, and other ancillary departments. This position will be part of the CTO Clinical Operations Unit and will report to the Deputy Director of the Clinical Trials Office.  

This individual must work collaboratively with CTO managers and ancillary services in program development and strategic planning- which includes participating in the organization and management of the new 3rd Floor HCC Research Infusion Suite and expansion of research services to satellite sites.  This individual will participate in the feasibility review process by reviewing protocols and determining the study patient flow and provision of center resources to promote protocol compliance and study participant retention.

Additionally, this nurse manager II will collaborate closely with other clinical operation program managers and the EPIC/Beacon build team members to ensure that study treatment plans are built in accordance with the protocol for newly activated and amended therapeutic protocols. The Nurse Manager II will have a key role in helping train and mentor new study coordinators and data managers in understanding oncology terminology and concepts.

This individual must be knowledgeable of Food and Drug Administration federal regulations, local regulatory agency policies, and international Good Clinical Practice Guidelines to ensure that the conduct of clinical research activities remain in good standing and research performance excels in quality and efficiency. Responsible for the establishment of clinical operation standard operating procedures and proper training and quality assurance initiatives.

Responsibilities:**(35%) Protocol Implementation and Support:
** Participates within the HCC CTO Research Allocation and Feasibility Team (RAFT) to read protocols and develop the best method for protocol implementation. Responsible for facilitating the interaction between HCC’s clinical research program and the clinical service line components.  When complex trials are identified by the RAFT and the HCC clinical research groups (CRG) that require additional nursing resources greater that what is provided as standard of care, this individual may be assigned to the study and provide study specific nursing services such as ECOG performance status assessments, vitals, EKGs, etc.

Additionally, the nurse manager will collaborate closely with other clinical operation program managers.  They will participate as a member of the CTO EPIC/Beacon build team and ensure that study treatment plans are built in accordance with the protocol for newly activated and amended therapeutic protocols. This individual will review study specific roadmaps to ensure that roadmaps are developed per the protocol and operational assessment determined by the CRG.

Will lead the Beacon build validation meetings. Will review protocol amendments and make changes to the roadmap as needed and per standard operating procedures. Utilizes CTO systems such as SharePoint and OnCore…
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