Clinical Regulatory Consultant

CK Group are recruiting for a Clinical Regulatory Consultant to join a dedicated and well established consulting company who are based in Munich on a permanent basis.

Location:

The role is based in Munich and requires 3 days/week on site

Role:

• Support 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.
• Provide strategic regulatory guidance to project teams on clinical development projects.
• Plan and execute the global regulatory development plan.
• Be responsible for the global agency interaction strategy.

Your Background:

• Educated to Ph.D. or master’s degree level in life sciences or a related field.
• Extensive experience in regulatory strategy throughout clinical development stages,
• Experience with EU and US Regulatory procedures and working with multiple regulatory authorities.
• Excellent communication and negotiation skills in English. German language skills are a plus.
• Strategic thinker, solution oriented and excellent task management and prioritisation skills.

Apply:

For more information, or to apply for this Clinical Regulatory Consultant position please contact Mary Bolt on 01246 457729 or email mbolt@ckgroup.co.uk. Please quote job reference 104626 in all correspondence.