Research Site Manager

The Research Site Manager is responsible for the overall leadership and direction of the facility’s research program, including, but not limited to, fiscal management, study and site operations, and oversight of day to day operations.

• Oversee clinical trial-related activities
• Ensure completeness and accuracy of data
• Problem solve clinical situations
• Assess organizational processes and identify areas for improvement
• Plan, facilitate, and present trial management issues and data status updates
• Provide oversight, leadership, and direction in the management and execution of trials
• Assess quality of data and performance of clinical trials
• Manage, monitor, and operate within allowed budget
• 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
• Work to ensure successful implementation of the EMR and optimization of processes to support clinical outcomes and patient experience
• Promote communication and accountability between staff and physicians
• Monitor billing colleagues and services, support financial reports and complete financial analysis to determine areas for improvement in financial outcomes
• Maintain competency and enhance professional growth and development through continuing education, conferences, and seminars
• Oversee all aspects of patient treatment associated with trial execution, including enrollment, patient consent, lab work, data entry, and drug storage/distribution
• Keep the executive team abreast of issues, progress, and risks related to trial operations and the overall clinic
• Assists in developing and executing internal and external strategies
• Responsible for the recruitment, hiring, training, development, and termination of colleagues, as necessary

• Bachelor’s Degree
• Registered Nurse - Must have a valid license as a Registered Nurse for the State of Nevada
• Knowledge of FDA guidelines and GCP
• Experience using clinical trial databases, electronic data capture, MS Access and MS Excel
• At least three years of experience in an oncology setting
• At least one year of experience supervising or managing others
• At least one year of experience in blood cancer/Bone Marrow Transplant (BMT)
• Research Certification (ACRP or CCRP) preferred

• 401k matching
• Health insurance
• Flight privileges
• Total Rewards package

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.