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Sarah Cannon Research Institute · 2 days ago

Research Site Manager

Las Vegas, NV

Full-time

Onsite

Mid, Senior Level

3+ years exp

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations focused on advancing therapies for patients. The Research Site Manager is responsible for the overall leadership and direction of the facility’s research program, overseeing clinical trial activities and ensuring compliance with guidelines while managing the research staff and operations.

Research

Responsibilities

You will oversee clinical trial-related activities completed/performed by the research staff to ensure completeness and accuracy as well as adherence to federal and state guidelines

You will problem solve clinical situations along with the research staff and the management team as they arise

You will assess the organizational processes associated with trial execution and identifies ways to improve and streamline internal procedures

You will plan, facilitate, and present trial management issues and data status updates at internal and external meetings

You will provide oversight, leadership, and direction in the management and execution of trials

You will assess quality of data and performance of clinical trials and develops action plans to address performance gaps

You will manage, monitor, and operate within allowed budget

You will review of all program billing outcomes and for working with billing staff and Sarah Cannon in addressing issues impacting financial outcomes and patient billing experience

You will work to ensure successful implementation of the EMR and optimization of processes to support clinical outcomes and patient experience

You will promote communication and accountability between staff and physicians

You will monitor billing colleagues and services, support financial reports and complete financial analysis to determine areas for improvement in financial outcomes

You will maintain competency and enhance professional growth and development through continuing education, conferences, and seminars

You will enhance operational effectiveness, emphasizing cost containment without jeopardizing innovation of quality of care

You will oversee all aspects of patient treatment associated with trial execution, including enrollment, patient consent, lab work, data entry, and drug storage/distribution

You will keep the executive team abreast of issues, progress, and risks related to trial operations and the overall clinic and you will meet frequently with all investigators

Assists in developing and executing internal and external strategies

Responsible for the recruitment, hiring, training, development, and termination of colleagues, as necessary

Qualification

Registered Nurse LicenseFDA guidelinesClinical trial databasesGCP knowledgeMS AccessMS ExcelOncology experienceSupervisory experienceResearch CertificationBlood cancer/BMT experience