Clinical Research Associate

IDR is seeking a Clinical Research Associate 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 Associate :

• Collaborate with the team to submit research projects for human subjects approval, including protocols, consent forms, and IRB applications.
• Manage internal documentation for contract execution and maintain communication with contracting officers and sponsors during budgeting and negotiations.
• Develop and monitor research project budgets, ensuring alignment with protocol requirements and institutional costs.
• Ensure compliance with IRB, FDA, OHRP, HIPAA, and other guidelines by maintaining high-quality regulatory files and submitting necessary paperwork.
• Coordinate site feasibility and initiation visits, and provide facility tours for research sponsors and other personnel.

Required Skills for Clinical Research Associate :

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