The Clinical Research Associate will support clinical research activities within research sites and assist with study and site start-up activities, data management, and site monitoring.
Requirements
- Bachelor’s degree (or higher) in nursing, health sciences or related field
- Minimum of two years of CRA experience, with clinical site monitoring experience preferred
- Experience with clinical trial contract and budget negotiations
- Finance experience preferred
- Strong oral and written communication skills
- Good understanding of FDA regulations related to clinical trials; GCPs and ICH Guidance
- Proven organizational skills and the ability to manage multiple priorities
- Strong computer skills
Benefits
- Full Time job
- Job location: Ridgefield, CT
- Job type: Full Time