Job Description

IDR is seeking a Clinical Research Coordinator to join one of our top clients in Los Angeles, CA. This role offers a unique opportunity to work onsite, fostering close collaboration with our client's team and immersing yourself in a dynamic work environment. If you are eager to be part of a growing organization with a team-oriented culture, please apply today!

• Engage in the design and execution of research projects, providing clinical research expertise and patient care as needed.
  
• Coordinate and manage research projects at both institutional and departmental levels, serving as an internal consultant for specific activities.
  
• Develop and maintain research infrastructure, including protocol writing, case report form development, and budget coordination.
  
• Ensure compliance with FDA, HSPC, HIPAA, and other agency guidelines by maintaining consent forms, case report forms, and other essential documents.
  
• Act as a liaison with Principal Investigators and pharmaceutical representatives, monitoring project progress and facilitating audits and study monitoring.
  

• Bachelor's degree is required.
  
• Minimum of 5 years of experience in clinical research, including IRB application procedures.
  
• Extensive experience in managing Phase I-IV clinical trials.
  
• Proficiency in protocol writing and conducting investigator-initiated trials.
  
• Preferred experience in Pharmaceutical/Biotechnology or Contract Research Organization (CRO) settings.
  

• Competitive compensation package
  
• Full Benefits; Medical, Vision, Dental, and more!
  
• Opportunity to get in with an industry leading organization
  
• Close-knit and team-oriented culture
  

• 25+ Years of Proven Industry Experience in 4 major markets
• Employee Stock Ownership Program
• Medical, Dental, Vision, and Life Insurance
• ClearlyRated's Best of Staffing® Client and Talent Award winner 12 years in a row

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