Jobs · Analyst · Washington

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

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