Summer Intern - Regulatory
Job description
About the Company
UroGen is a biotech company dedicated to developing and commercializing innovative solutions that treat urothelial and specialty cancers. We are fundamentally changing the way patients are treated for urologic cancers.
Watch our New Horizons in Bladder Cancer event and discover why it’s an exciting time to join UroGen® Pharma. Join us and be part of the team that will redefine the future of urological cancer treatment. Behind every UroGen innovation is the inspiration to empower uro-oncology patients with life-changing treatments.
At UroGen, our people are our greatest asset. We cultivate a culture built on collaboration, creativity, and continuous growth. UroGen is a dynamic, rapidly expanding organization with an unwavering focus on improving the lives of patients because they deserve better.
Location: Princeton (remote acceptable) Job Summary: Support Project Management and Regulatory Operations in the management of regulatory submission, R&D projects, and the maintenance of Veeva RIM and SmartsheetJob requirements
Current College Student. Focus in sciences preferred but not mandatory.Job responsibilities
- Track status of planned and completed regulatory submissions, ensure Veeva RIM is up to date.
- Attend NDA and R&D Project Team meetings, track project status and update major deliverables dashboard and other project documentation.
- Support the implementation of Project Management/Regulatory Operations improvement initiatives such as Smartsheet implementation, Veeva Reports, submissions management workflows, etc.