Tech Stack

Description

You will support regulatory review activities for clinical studies, manage contracts and invoices, maintain tracking tools and archives, assist with submission workflows in Veeva, and participate in regulatory meetings. This is a chance to learn drug development in a clinical-stage oncology company.

Requirements

• Pursuing bachelor's/MS/PhD in life science, pharmacy, regulatory science or related field
• Basic understanding of drug development
• Attention to detail and organizational skills
• Good verbal and written communication skills
• Proficiency in Microsoft Office (Word, Excel, PowerPoint)

Responsibilities

• Support regulatory review activities for site activation across clinical studies
• Manage Regulatory Affairs contracts and invoices
• Maintain regulatory query tracker and archive regulatory documents
• Support regulatory submission workflows in Veeva
• Co-host Regulatory Sub-Team meetings and document action items