Senior Clinical Research Coordinator - Hematology/oncology (santa Monica)

Uclahealth

Santa Monica, CA, United States
$82,705.68 - 133,068.24 annually; not specified; n...
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Clinical research protocol management
Patient interaction and communication
Regulatory compliance and documentation
** UCLA Health is seeking a Senior Clinical Research Coordinator specializing in hematology/oncology to oversee clinical trial operations. The ideal candidate will have extensive experience in clinical research, strong communication skills, and the ability to manage multiple priorities effectively. **

Job Summary

  • The Senior Clinical Research Coordinator is responsible for the operational management of clinical research activities, ensuring accurate and timely completion of study protocols.
  • This role requires strong project management skills, the ability to work with various stakeholders, and a deep understanding of clinical research concepts and regulations.
  • The position offers a flexible hybrid work schedule and a competitive salary range, with opportunities for supervision and training of others.

Matching Summary

Match Score: 75

** UCLA Health is seeking a Senior Clinical Research Coordinator specializing in hematology/oncology to oversee clinical trial operations. The ideal candidate will have extensive experience in clinical research, strong communication skills, and the ability to manage multiple priorities effectively. **

Salary

$82705.68 - 133068.24 Annually; Not specified; Not specified

Skills & Requirements

Must-have

  • Clinical research protocol management
  • Patient interaction and communication
  • Regulatory compliance and documentation
  • Interpersonal and team collaboration skills
  • Proficiency in Microsoft Suite

Nice-to-have

  • Adaptability to changing demands
  • Attention to detail in fast-paced environment
  • Learning and growth mentality
  • Creative problem-solving abilities

Key Requirements

  • Minimum 4+ years of clinical research experience
  • Experience with FDA processes and procedures
  • Knowledge of local and external IRBs
  • Experience with clinical trials budgeting

Work Rights

Not specified

Tailored Resume

Cover Letter