Full-Time

Univ – SISU Administrative Director-Hollings Cancer Center

Posted on 11/21/2024

Medical University of South Carolina

Medical University of South Carolina

Compensation Overview

$83.2k - $154kAnnually

Mid, Senior

Charleston, SC, USA

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Requirements
  • Bachelor's Degree; Preferably Masters.
  • five years relevant program management experience.
  • Prefer prior oncology clinical research experience, particularly in regulatory.
Responsibilities
  • This role will work with the HCC’s Research Programs and clinical leaders in the development and completion of all HCC-driven investigator-initiated treatment trials and other IITs managed by the HCC CTO.
  • He/she will serve as the administrative chair of the Hollings Advisory for Rapid Translation (HART), which is an executive board of the Hollings Cancer Center that oversee the trial pipeline of clinical trials derived from HCC members and HCC science.
  • The role will lead the SISU teams to provide efficient and high-quality activation services and sponsor maintenance activities.
  • The SISU Administrative Director will track all IIT projects, monitor performance metrics, and effectively address or escalate issues to HCC’s executive leadership.
  • He/she must know clinical trial operations standards, budget development and research finance billing compliance, and local IRB, DSMC, and FDA policies and procedures.
  • Project management skills are required to track all SISU procedures from concept to completion.
  • Effective and professional communication skills are needed to work across the MUSC enterprise, industry sponsors, and IIT academic sub-sites across the country.
  • Participates within the HCC Translational Cancer Teams and Disease Focus Groups to represent the CTO and learn and support the creation of new clinical trial ideas.
  • Shares findings with the CTO Director and assists in presenting information and initiatives at that Clinical Research Executive Committee, HCC Leadership meetings and monthly HCC Research Program meetings.
  • The SISU operating budget is approximately $1 million annually and the team manages a growing portfolio of IITs study accounts of multicenter and single center early phase clinical trials.
  • The SISU Administrative Director must demonstrate skills to effectively develop IIT study budgets and review and negotiate contract language (in collaboration with MUSC central contract office).
  • He/she will assist clinical researchers in developing proposals for external and internal trial funding and provides program management to investigators developing new investigator-initiated research letters of intent or grant applications.
  • In collaboration with the SISU scientific director, he/she will communicate trial-specific and program needs to stakeholders within MUSC and external stakeholders such as pharmaceutical sponsors, biotech companies and potential philanthropic donors or HCC advisory board members in efforts to secure the essential resources for IIT implementation.
  • The position will oversee the SISU fiscal activities of the HCC CTO pre-award coordinator to ensure that every IIT is set-up with the proper research billing compliance standards such as a prospective reimbursement analysis and research billing grid.
  • When external service agreements are needed for the completion of an IIT activities (e.g. drug distribution, lab analysis, etc.), this role will support the PI in overseeing the procurement and budget management of the professional services.
  • This position will also work closely with the CTO finance manager and post-award team, or the PI’s grant administrator to ensure that funding partners IITs are properly invoiced and any annual NIH progress report is completed.
  • External peer review grant management knowledge will be essential to support the PI in developing NIH draft budgets and supporting the PI in the completion of grant reporting requirements.
  • Program development responsibility will span human resource responsibilities, quality assurance, and continuous process improvement and strategic planning.
  • As the SISU supervisor, he/she will support position SISU hiring, performance evaluation, mentorship and education.
  • This role will work with the coordinators and, as applicable, other University departments to develop policy and procedures and adjust SOPs as new directives or system changes apply.
  • He/she will support and maintain training of SISU employees and sponsor-investigators.
  • He/she will create and support a quality assurance program for SISU clinical research activities.
  • With minimal supervision, he/she will monitor non-compliance with national performance benchmarks and relevant local and federal regulations and identify areas for improvement and implement strategies for corrective actions.
  • In collaboration with the CTO, IRBs, Office of Clinical Research, and other institutional partners, this role will assure that SISU policy and procedures meet the HCC DSMP and other applicable federal and local regulations.
  • It will be important to stay abreast of IIT program service trends among other NCI Designated cancer centers and develop strategic plans to enhance the SISU program.
  • He/she will also work with HCC leadership to ensure that strategies are in place to promote robust growth and productivity of the HCC IIT portfolio.
  • Provide project management of special activities and other duties as assigned.
Medical University of South Carolina

Medical University of South Carolina

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