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 and thrive in a team-oriented culture, please apply today!
Position Overview/Responsibilities for the Clinical Research Coordinator:
• Engage in the design and execution of research projects, providing clinical research expertise and patient care as needed. • Oversee specific aspects of research infrastructure, coordinating projects at both institutional and departmental levels. • Serve as an internal consultant, communicating project status and areas for improvement to leadership. • Implement department-wide initiatives, such as research quality management and clinical trial recruitment. • Ensure compliance with FDA, HSPC, HIPAA, and other guidelines, managing consent forms, case report forms, and IRB submissions.
Required Skills for Clinical Research Coordinator:
• 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 handling investigator-initiated trials. • Preferred experience in Pharmaceutical/Biotechnology or Contract Research Organization (CRO) settings.
What's in it for you?
Competitive compensation package
Full Benefits; Medical, Vision, Dental, and more!Opportunity to get in with an industry-leading organizationClose-knit and team-oriented cultureWhy IDR?
25+ Years of Proven Industry Experience in 4 major markets
Employee Stock Ownership ProgramMedical, Dental, Vision, and Life InsuranceClearlyRated's Best of Staffing® Client and Talent Award winner 12 years in a row