OPIS is seeking a Director of Regulatory and Submissions to lead a high-performing team and ensure client projects meet rigorous standards. This pivotal role involves ensuring compliance and quality across a dynamic, fast-growing Clinical Research Organization, working with regulatory authorities globally. The position is fully remote and based in one of the European countries.
Requirements
- Lead global regulatory operations
- Oversee submissions to Competent Authorities and Ethics Committees
- Manage Clinical Trial Applications
- Serve as the liaison for regulatory agency interactions
- Build a culture of growth, mentorship and high performance
- Conduct skill-development activities, annual reviews, and foster career advancement
Benefits
- Competitive salary
- Opportunity to be part of a company that values growth, innovation, and customer success