Offer summary
Qualifications:
Bachelors in Business or Science-related field, Masters in Business or Science-related field, 5-10 years leading risk assessments in pharmaceutical industry, Experience with cross-functional teams, Knowledge of clinical trial management process.
Key responsabilities:
- Create and manage risk assessments
- Facilitate risk management and control communication
- Collaborate with stakeholders to analyze risks
- Draft, maintain, and archive risk documentation
- Support clinical development optimization with RBQM model