About this role
Role Overview
- Lead or contribute to development of Clinical Development (CD) strategy and plan
- Support development and implementation of the Clinical Development Plan (CDP)
- Collaborate with internal/external partners & stakeholders
- Participate in meetings regarding early development/Phase I studies
- Ensure strategic and operational alignment of the CDP with the relevant CD strategy
- Work with CST members to develop CDP components
Requirements
- Board Certified/Board Eligible (or its equivalent) MD (MBBS), MD(MBBS)/PhD physician in gastroenterology or hepatology
- 5+ years of post-grad relevant clinical/scientific research and/or clinical trial experience
- 3 or more years of experience in biopharmaceutical clinical development with late stage drug development
- 3+ years of medical monitoring experience within the life sciences space
- 2+ years of experience engaging with clinical sites, PIs, KOLs etc
- Solid understanding of Phase II – III drug development
- Significant contributions to an organization’s drug development
- Experience in scientific writing (e.g. manuscripts, grants, scientific protocols, health authority documents)
Benefits
- Discretionary annual bonus available based on individual and Company performance
- Relocation support provided for this position