Our client, a leading life sciences consultancy based in Munich, is seeking a highly experienced Clinical Regulatory Affairs Consultant to join their team of experts. With more than two decades of success supporting drug and device development projects across Europe, North America, Asia and beyond, they’re known for solving complex regulatory challenges and pioneering innovative solutions.
This position supports cross-functional development teams working on small molecules, biologics, and ATMPs across all phases—from early research through to clinical development and global marketing applications (MAA, NDA, BLA).
Key Responsibilities:
* Provide strategic regulatory guidance across global drug development programs
* Lead clinical development strategy within interdisciplinary project teams
* Design and execute global regulatory development plans
* Drive global agency interactions and engagement strategy
Candidate Profile:
* Advanced degree in life sciences, medicine, or veterinary medicine
* 10+ years’ experience in pharmaceutical development
* Strong expertise in clinical development strategy and regulatory planning (beyond operational or people management roles)
* Ability to navigate complex development scenarios and communicate clearly with stakeholders
* Ideally experienced across diverse pharma organisations and/or regulatory bodies
* Familiarity with both EU and US procedures is a plus
What’s on Offer:
* A dynamic, collaborative work environment in central Munich
* Flexibility to work hybrid with a preference for 3 days/week onsite (relocation support available)
* Attractive compensation package with performance-based bonus
* Opportunity to make a real impact in a nimble, high-performing team
Interested in learning more?
Contact Rhiannon Ross at rhi@greenlsr.com for a confidential conversation or apply now through our LinkedIn page.