Job Summary
A company is looking for a Sr. Associate - Central Clinical Services.
Key Responsibilities
- Oversee communication and management of activities for potential participants and study partners
- Monitor scheduling, logistics, and technology for participant assessments and related entities
- Provide oversight to vendors and ensure compliance and quality throughout study timepoints
Required Qualifications
- Bachelor's degree in a scientific or health-related field
- 2+ years of clinical research experience or relevant experience preferred
- Understanding of the clinical development paradigm and site activation processes
- Applied knowledge of project management processes
- Experience in a compliance-driven environment
Comments