Community Site Research Manager
Fred Hutch · Seattle, WA · Yesterday
Analyst$99k–$157k/yrFull-time
Responsibilities
- Oversee study startup at community sites, working closely with central teams to move studies from feasibility through activation.
- Ensure research protocols are carried out smoothly across the full study lifecycle, from feasibility to closeout.
- Support integration of research activities into everyday clinical workflows to minimize disruption to patient care.
- Maintain adequate participant coverage and engagement across community sites by monitoring enrollment capacity, supporting recruitment and retention strategies, and proactively addressing barriers to participant access and study participation.
- Manage and support site-based research staff (coordinators and data roles) to ensure quality and compliance.
- Build and maintain strong relationships with community providers, site leadership, and external partners (e.g., sponsors, CROs).
- Implement and maintain standard operating procedures, promoting consistency across locations and alignment with clinical trial coordination.
- Plan staffing and support hiring, onboarding, and development of research staff at community locations.
- Monitor performance, identify issues, and implement improvements to site operations, quality, and efficiency.
- Track and report key metrics (e.g., startup timelines, enrollment, data quality) and ensure compliance with all regulatory and institutional requirements.
Qualifications
- Bachelor's degree/equivalent qualification or experience
- 4 years’ experience in the conduct of interventional, treatment, and/or FDA-regulated clinical trials, preferably oncology trials
- At least 2 years’ experience directly or indirectly managing personnel and training team members
- Knowledge of FDA regulations, GCP guidelines, and other applicable federal regulations
- Excellent interpersonal skills with the ability to build strong relationships with a diverse group of stakeholders
- Experience working with EHR systems
- Experience working with clinical trial management system
- Excellent oral and written communication skills