**Associate Clinical Trials Regulatory Manager**

**EMEA**

**Homebased**

**Job Summary**

The Associate Clinical Trials Regulatory Manager provides regulatory support and oversight for clinical trial submissions across global programs. This role is responsible for preparing and reviewing regulatory documentation, managing submissions, ensuring regulatory compliance, and supporting clients and internal stakeholders throughout the clinical trial lifecycle. This is not a people manager role, but a process management position.

**Key Responsibilities**

+ Serve as the Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects and programs.
+ Provide regulatory oversight and strategic guidance to internal and external stakeholders.
+ Review scientific and regulatory documentation, conduct gap analyses, and provide recommendations.
+ Author and/or review key regulatory documents, including Investigational Medicinal P...