Clinical Research Manager

• Direct planning and implementation of clinical research protocols within K-12 settings
• Ensure high-quality execution of programs focused on student social-emotional and behavioral success
• Identify and solicit new internal and external research opportunities
• Promote center capabilities and recommend strategic program enhancements to leadership
• Develop and maintain clinical research policies, standard operating procedures, and operational guidelines
• Compile audits and document research data for compliance with institutional policies and procedures
• Compose, assemble, and submit grant proposals and research protocols
• Supervise at least 2.0 FTE clinical research staff, including hiring, performance management, and professional development
• Manage program functioning and fiscal health through budgets, expenditure monitoring, and resource optimization
• Plan staff implementation and ongoing quality review of clinical research trials or programs
• Collaborate with faculty, staff, investigators, and school/community stakeholders under Principal Investigator supervision

• Demonstrated experience coordinating and managing clinical research trials or programs involving human subjects
• Experience exercising supervisory authority, including hiring, performance management, and professional development of staff
• Ability to compose, assemble, and submit grant proposals and research protocols in accordance with federal, state, and institutional regulations
• Knowledge of clinical research policies and procedures, including IRB standards and data privacy such as HIPAA or FERPA
• Experience developing and monitoring program budgets, including reviewing and approving expenditures
• Strong written and verbal communication skills
• Master's degree required
• Preferred degree in education, psychology, social services, education, school psychology, social work, or a related field
• Eligibility to work in the United States
• Successful applicants may be subject to a criminal background check
• Three professional references required
• Resume/CV and cover letter required

Demonstrates expertise in managing clinical research protocols and trials within K-12 settings, ensuring compliance with regulations and promoting student success through effective program execution and staff supervision.

• Clinical Research Management
• Grant Proposal Development
• Budget Development and Monitoring
• Supervisory Experience
• Knowledge of IRB Standards

• Clinical Research Protocols
• Program Evaluation
• Data Compliance
• Expenditure Monitoring
• Research Data Documentation
• Policy Development
• Standard Operating Procedures
• Human Subjects Research
• Program Enhancement
• Audit Compilation

• Strong Written Communication
• Strong Verbal Communication

• K-12 Education
• Social-Emotional Success
• Behavioral Success
• HIPAA
• FERPA
• Institutional Regulations
• Performance Management
• Professional Development
• Stakeholder Collaboration
• Criminal Background Check