Clinical Regulatory Consultant in München (81249), Bayern

ARM is proud to collaborate with a prestigious consultancy firm in the life science industry, presenting an exceptional permanent position based in Munich, Germany (relocation support offered). They are offering this on a hybrid model where they will require someone onsite at least 3 days per week. This role offers the unique opportunity to work closely with esteemed clients and diverse projects.

This position supports cross-functional development teams for innovative drug development (i.e. small molecules, biologicals, ATMPs) at any stage of development - from research throughout clinical development until MAA, NDA/BLA.

Responsibilities include, but are not limited to:

• Providing strategic regulatory guidance to project teams
• Covering clinical development in the project teams
• Planning and executing the global regulatory development plan
• Responsible for the global agency interaction strategy

Requirements:

• Exceptional experience in pharmaceutical development.
• Practical experience in strategic clinical development and regulatory strategy.
• Ability to support with complex development scenarios.
• Experience with both EU and US regulatory procedures would be preferred.

If you are interested in discussing this further please apply directly, or alternatively contact me on or +44 23 9222 8211

Disclaimer:

This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission.