About this role
About the Role The role supports the development of the Clinical Development Plan (CDP) for assigned molecule(s) or indication(s) within Roche’s metabolism/obesity/diabetes programs. It focuses on gathering and analyzing data to inform CDP strategy and collaborating with CST and sub-teams to develop plan components such as analytics/data strategy, KOL development, and publications strategy. What You'll Do
- Participate in development of the CD plan for assigned molecule(s)/indication(s)
- Gather and analyze data and information necessary to create the CD plan
- Work with CST members and relevant sub-teams to develop CD plan components (e.g., analytics/data strategy, KOL development, publications strategy, etc.)
- Work with CST and other relevant teams to develop and provide information and input What We're Looking For
- MD required
- Therapeutic knowledge within metabolism, obesity, and diabetes with relevant clinical, scientific, and clinical trial/development experience
- Experience with data analysis, interpretation, and determining clinical relevance
- Experience publishing results of scientific studies in peer-reviewed journals preferred
- Knowledge of medical aspects of GCP, ICH, FDA, EMA, and other guidelines; regulatory familiarity preferred
- 2+ years of post-graduate academic or clinical experience
- Up to 30% global travel
- Academic/teaching background is a plus; other relevant experiences may be applicable