Clinical Research Project Manager

• Turn project concepts into executable plans, defining scope, goals, milestones, budgets, and success measures.
• Manage cross-functional execution across clinical, research, finance, legal, and external partners for clinical studies and grant-funded research.
• Use modern LLM and agentic tools (e.g., Claude Code, Codex) to improve project planning, documentation, analysis, and operational workflows.
• Build reusable project-management systems, templates, and workflows to strengthen organizational execution.

This role directly advances CASPR's mission to reduce the global burden of addiction by ensuring that clinical research projects—including a post-incarceration GLP-1 randomized trial—are executed effectively, accelerating the development of scalable, science-based interventions.

• 5+ years of experience in project management, clinical research operations, healthcare, scientific research, or research administration.
• Demonstrated experience managing complex, multi-stakeholder projects with interdependent workstreams, deadlines, budgets, and deliverables.
• Proficiency using modern LLM and agentic tools (e.g., Claude Code, Codex) to plan projects, synthesize information, and create efficient workflows.
• Strong organizational skills, attention to detail, and ability to communicate clearly with senior leaders and external partners.

Compensation and benefits are not specified in the posting. The role offers the opportunity to work with a mission-driven nonprofit at the forefront of addiction science, with exposure to cutting-edge AI tools and collaboration with leading experts.

CASPR is a nonprofit organization dedicated to reducing the global burden of addiction through scalable science-based interventions, advancing evidence-based practices, running research and clinical studies, and shaping policy to find a cure for substance use disorders.