Sr. Clinical Research Coordinator - Radiation Oncology

Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health's world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.

The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout. This role is well-suited for an experienced research professional who can lead study activities, manage priorities, and ensure high-quality, compliant execution across complex research projects.

Key Responsibilities:

• Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials
  
• Ensure study protocols and procedures are carried out accurately, safely, and on schedule
  
• Coordinate timelines, prioritize tasks, and support project management needs
  
• Train and supervise research staff as needed
  
• Collaborate with Principal Investigators, sponsors, and internal and external partners on compliance, financial, and operational aspects of studies
  

Salary: $6,892.14 - $11,089.02 monthly

Required:

• Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience
  
• Ability to work flexible hours to accommodate research deadlines.
  
• Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.
  
• Strong written communication skills, ability to compose advanced correspondence and manage large file systems.
  
• Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.
  
• Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.
  
• Advance knowledge of the clinical research regulatory framework and institutional requirements.
  
• Ability to supervise and delegate clerical work as needed.
  
• Advanced knowledge of Good Clinical Practice (GCP) for clinical research.
  

Preferred:

• Working knowledge of FDA applications