The Clinical Research Operations Manager will support the overall design, planning, implementation and management of the clinical research program at the LSUHSC Cancer Center. They will provide oversight for clinical research operations, working alongside counterparts in regulatory affairs, program management, data management, quality assurance, and systems administration to develop annual measurable goals and objectives for the research program. The incumbent will supervise the Disease Group Supervisor, Regulatory Manager, and Data Management Supervisor as related to performance improvement activities by contributing ideas, experience, and expertise to promote efficiency and quality outcomes for the Cancer Center.
The Clinical Research Operations Manager will be responsible for monitoring budgets and study invoices and providing reports to Cancer Center Administration, Cancer Center Clinical Trials Office (CC-CTO) Directors and LCMC partners and affiliates. They are expected to interact with the LSUHSC-NO Compliance Office to ensure studies are conducted in accordance with internal and external policies, procedures, regulations, and guidance documents. The incumbent will also consult with research leadership to ensure applicable, efficient, and effective research processes while making innovative and thoughtful recommendations and improvements to increase efficiency while ensuring compliance with research protocols, IRB, and sponsored research guidelines.