N-Power Medicine, Inc. is a healthcare and biotechnology company developing tools to improve oncology drug development and clinical research. Its N-Power Platform brings together standardized data collection, real-time analysis, and expert research support to help oncology practices participate more effectively in clinical trials. The company works with oncologists, biopharmaceutical organizations, and patient advocacy groups to expand trial access, generate stronger real-world evidence from routine care, and support the development of high-performing research sites.
Senior Director of Clinical Research Operations (Remote, U.S.)
Lead distributed oncology clinical trial operations for N-Power Medicine across network practices. Build staffing models, clinical workflows, training programs, and performance systems that support scalable execution.
Description
- Lead the operating model for N-Power Medicine’s clinical research execution across network practices
- Develop a scalable staffing model based on health system profiles, clinical programs, enrollment goals, and patient volume
- Establish CRS productivity and success measures aligned with business and pharmaceutical customer delivery goals
- Create dashboards and reporting routines that provide visibility into team and site performance
- Analyze performance data to identify capability gaps and target training investments
- Develop playbooks, SOPs, and management routines for a consistent distributed field organization
- Manage the Clinical Operations team directly
- Bring study startup, TMF management, documentation, site and IRB coordination, and site monitoring into an integrated function
- Develop scalable training and professional development infrastructure
- Prepare onsite staff to communicate N-Power Medicine’s mission and value proposition to practice partners
- Act as the escalation point for site-level relationship risks
- Help implement new initiatives and workflow changes across the network
- Collaborate with Network Operations leaders and cross-functional teams to align priorities with the broader network strategy
Requirements
- At least nine years of experience in clinical research operations
- Hands-on experience managing oncology clinical trials
- Demonstrated success leading a distributed, multi-site workforce at scale
- Deep knowledge of oncology research and practice workflows, including academic and community research environments and practice administration
- Experience creating repeatable playbooks, SOPs, and processes for growing teams and programs
- Experience developing staffing models, capacity plans, and KPI reporting frameworks from the ground up
- Experience designing training and development programs for distributed clinical teams
- Bachelor’s degree or equivalent professional experience
- Excellent written and verbal communication skills
- Collaborative, hands-on leadership in fast-moving environments
- Familiarity with CTMS, EDC, or comparable clinical trial systems in site-level workflows preferred
- Willingness to travel as needed to support regional teams, up to 25%
- Current authorization to work full-time in the United States
- Ability to pass all applicable state-specific background checks and screenings
Benefits
- Equity offered at hire
- Discretionary annual bonus may be available based on company performance
- Company benefits
- Balanced and flexible work environment
- Competitive industry benefits
- 401(k) plan