Clinical Research Coordinator - Hematology/oncology (santa Barbara)

Uclahealth

Santa Barbara, CA, United States
Base: $36.37 - $58.52 hourly; bonus/equity: not sp...
On-site
Implementing clinical research activities
Ensuring compliance with fda cfr regulations
Managing multiple project deadlines efficiently
UCLA Health is seeking a Clinical Research Coordinator specializing in Hematology/Oncology to manage clinical research activities in Santa Barbara, CA. The ideal candidate will possess a Bachelor's degree and have 1-3 years of experience in clinical research coordination, along with strong communication and organizational skills

Job Summary

  • The Clinical Research Coordinator supports the operational management of clinical research activities throughout the entire study lifecycle.
  • This role requires close collaboration with the Principal Investigator, ancillary departments, and external institutions to ensure compliant study conduct.
  • Candidates must possess strong organizational capabilities to manage competing deadlines while adhering to FDA Code of Federal Regulations and ICH Good Clinical Practice.

Matching Summary

Match Score: 85

UCLA Health is seeking a Clinical Research Coordinator specializing in Hematology/Oncology to manage clinical research activities in Santa Barbara, CA. The ideal candidate will possess a Bachelor's degree and have 1-3 years of experience in clinical research coordination, along with strong communication and organizational skills.

Salary

Base: $36.37 - $58.52 Hourly; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • implementing clinical research activities
  • ensuring compliance with FDA CFR regulations
  • managing multiple project deadlines efficiently
  • collaborating with principal investigators and sponsors
  • preparing clinical trial budgets

Nice-to-have

  • strong verbal and written communication skills
  • ability to adapt to changing job demands
  • experience navigating numerous software programs
  • professional handling of confidential information
  • flexible availability for off-site visits

Key Requirements

  • Bachelors Degree or 1-3 years experience
  • Working knowledge of FDA CFR and ICH GCP
  • Mathematical skills for budget preparation
  • Ability to handle confidential material information
  • Willingness to travel for meetings and conferences

Work Rights

Not specified

Tailored Resume

Cover Letter