Regulatory Affairs Associate
reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. Regulatory Affairs Associate 2 to 4 years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts.
- To understand the regulatory reputed company, including regional trends, for various types of applications and procedures for small and large molecules across reputed company reputed company.
- Support authoring Annual reports/Renewal experience US/ EU/Brazil/LATAM/China.
- Liaise closely with cross-functional members with reputed company product responsibilities.
- Knowledge of change evaluation according to country guidelines
- Experience in managing lifecycle activities in the EU markets would be preferrable
- Knowledge of CTD guidelines
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