Senior Regulatory Affairs Manager
6 days ago
About Us
We are a fast-growing, dynamic company dedicated to transforming the lives of people with cancer and other serious diseases through Knock-Your-Socks-Off (KYSO) antibody medicines. Our core purpose guides our unstoppable team to strive towards improving patient lives through innovative and differentiated antibody therapeutics.
The Role and Department
In this role, you will assume responsibility for the EU/ROW regulatory strategy, closely collaborating with the Global Regulatory Team on one or multiple compounds in early or late-stage development.
Key Responsibilities
- Act as EU/ROW regulatory lead and EMA contact person for assigned project(s)
- Represent RA in the Clinical Trial Teams and ensure oversight and progress of multiple clinical trial submission activities
- Evaluate competitive landscape and various regulatory mechanisms to optimize product development and expedite the path to market in EU/ROW
Requirements
- A minimum of Bachelor's degree or equivalent in scientific discipline or health-related field
- Minimum of 7-8 years of experience in Regulatory Affairs, preferably in development phase
- Significant experience in proactively planning and executing complex clinical submission strategies
- Solid understanding of drug development and EU regulatory mechanisms
- Prior experience leading health authority meetings with the EMA or other health authorities, as well as experience with PIPs
- Strong project management skills
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