About this role
Role Overview
- Design and run global clinical trials
- Contribute to protocol development and study reporting
- Review publications and support labelling updates
- Engage with regulatory agencies and external thought leaders
- Ensure compliance with regulations and safety standards
Requirements
- Medical Doctor
- Board eligible or certified in appropriate specialty/subspecialty
- Fluent in English; both written and verbal communications
- Demonstrated knowledge of drug development process
- Experience of international oncology practice
- In depth knowledge of breast oncology
- Experience with CDK 4 & 6 inhibitors
- Clinical research or pharmaceutical medicine experience preferred
- Ability to engage in domestic and international travel
Benefits
- Embracing diversity
- Opportunities for philanthropy and volunteerism