About this role
Role Overview
- Manage and provide oversight for global public disclosure of clinical trial data
- Investigate & gather global requirements
- Implement processes for ensuring accuracy and alignment of clinical data
- Work globally & cross-functionally to align procedures
Requirements
- Bachelor’s degree
- 4 years submitting clinical trial registrations on behalf of sponsors
- 2 years preparing and presenting to peers and stakeholders
- 2 years working in collaborative, cross-functional teams
- 1 year serving as project manager in the pharmaceutical industry
Benefits
- paid time off (vacation, holidays, sick)
- medical/dental/vision insurance
- 401(k) to eligible employees
- participation in short-term and long-term incentive programs