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!
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.
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.
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 conducting 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 organization
Close-knit and team-oriented culture
Why IDR?
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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