Principal Clinical Regulatory Affairs Consultant

Green Life Science; München; Hybrid; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

A leading life sciences consultancy in Munich is seeking a highly experienced Principal Clinical Regulatory Affairs Consultant. The role involves providing strategic regulatory guidance, leading clinical development strategy, and engaging with global agencies. The ideal candidate will have over 10 years of pharmaceutical development experience and an advanced degree in life sciences or related fields. This position offers a dynamic work environment, flexibility, and a competitive compensation package.

Leistungen

Flexibility to work hybrid with a preference for 3 days/week onsite

Attractive compensation package with performance-based bonus

Qualifikationen

• 10+ years’ experience in pharmaceutical development.
• Strong expertise in clinical development strategy and regulatory planning.
• Ability to navigate complex development scenarios.

Aufgaben

• Provide strategic regulatory guidance across global drug development programs.
• Lead clinical development strategy within interdisciplinary project teams.
• Design and execute global regulatory development plans.

Kenntnisse

Regulatory planning

Clinical development strategy

Communication

Stakeholder engagement

Ausbildung

Advanced degree in life sciences, medicine, or veterinary medicine

Jobbeschreibung

Principal Clinical Regulatory Affairs Consultant

Principal Clinical Regulatory Affairs Consultant

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Ex-industry Regulatory professional and Principal Consultant for Green Life Science

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 [e-mail] for a confidential conversation or apply now through our LinkedIn page.

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Legal and Strategy/Planning

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Business Consulting and Services

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