Offer summary
Qualifications:
More than 6 years in Clinical Trial Regulatory, Experience leading global regulatory projects, Knowledge of EU-CTR 536/2014 preferred, Project management knowledge, Proficiency in local language.Key responsabilities:
- Support global strategies and ensure compliance
- Coordinate submission of Core dossiers
- Manage flow of information and problem-solving
- Review technical documents for regulatory compliance
- Interface with project teams and regulators