Senior Director, Clinical Research Operations

. Build and lead the full operating model for N-Power Medicine’s clinical research execution across network practices .

Posted 9/25/2026full-timeRemote • United StatesSenior💰 $215,000 - $270,000 per yearWebsite

Key responsibilities & impact

Build and lead the full operating model for N-Power Medicine’s clinical research execution across network practices
Build a repeatable and scalable staffing model tied to health system profile, clinical programs, enrollment targets, and patient volume
Define CRS productivity and success metrics tied to business and pharma customer delivery targets
Build dashboards and reporting cadences for team and site performance visibility
Use performance data to identify skill gaps and direct training investment
Build playbooks, SOPs, and management cadence for a consistent distributed field team
Directly manage the Clinical Operations team
Integrate study startup, TMF management, documentation, site/IRB coordination, and site monitoring into the function
Build scalable training and development infrastructure
Train onsite staff to represent N-Power Medicine’s mission and value proposition to practices
Serve as escalation point for site-level relationship risks
Support rollout of new initiatives and workflow changes across the network
Partner with Network Operations leadership and cross-functional teams to align priorities with broader network strategy

What you’ll need

9+ years of experience in clinical research operations
Direct, hands-on oncology clinical trial experience
Proven success managing a distributed, multi-site workforce at scale
Strong experience in oncology research and practice workflows, including academic/community research workflows and practice business administration
Demonstrated ability to build repeatable playbooks, SOPs, and processes as teams and programs grow
Experience building staffing models, capacity plans, and KPI/reporting frameworks from scratch
Experience designing training and development infrastructure for a distributed clinical workforce
Bachelor’s degree or equivalent professional experience
Exceptional written and verbal communication skills
Collaborative, hands-on leadership in dynamic environments
Familiarity with CTMS, EDC, or similar clinical trial systems as they relate to site-level workflow (preferred)
Travel expected as needed to support regional teams, up to 25%
Currently authorized to work in the U.S. on a full-time basis
Ability to successfully pass all applicable state-specific background checks and screenings

Comp & perks