Regulatory Affairs Specialist
We are seeking a highly skilled Regulatory Affairs Specialist to join our team in supporting the development of life-transforming medicines. As part of our global network, you will play a pivotal role in ensuring compliance with emerging legislation and regulations.
About the Role:
* To develop and implement EU-appropriate regulatory strategies for clinical development and product approvals.
* Provide leadership on both late- and early-stage clinical development processes to ensure timely study conduct.
* Leverage your expertise to oversee Marketing Authorization Application (MAA) processes and secure timely product approvals.
This is an exciting opportunity for a detail-oriented professional who thrives in fast-paced environments. If you have experience working with EU regulatory systems, enjoy collaborating with cross-functional teams, and excel at managing compliance issues, we encourage you to apply.
The ideal candidate will hold an advanced degree in a scientific field and have at least 5 years of experience in regulatory affairs. Experience with EU national agencies or EMA is preferred but not required.