About this role
Role Overview
- Supports the Clinical Study Lead (CSL) in clinical trial delivery
- Takes responsibility for areas of clinical trial delivery
- Works with study teams and external vendors (CROs)
- Involves feasibility, planning, initiation, maintenance, and closeout of clinical projects
- Contributes to risk assessment and mitigation strategies
- Oversees and provides input to study documentation development
- Reviews site-level informed consents and patient-facing study start-up materials
- Monitors recruitment and retention, data quality metrics, and issues
- Manages aspects of study close-out activities
Requirements
- Minimum of Bachelor's degree
- 4+ years of relevant clinical trial experience
Benefits
- Health and wellness programs (including medical, dental, vision, life, and disability insurance)
- Fitness centers
- 401(k) company match
- Family support benefits
- Equity awards
- Annual bonuses
- Paid time off
- Paid leaves (e.g., military and parental leave)