**Internal Clinical Research Associate – Remote**

As an Internal Clinical Research Associate, you will support key clinical trial activities from site activation through study closeout, helping ensure studies are conducted in accordance with regulatory requirements, quality standards, and clinical research best practices.

**What You Will Do**

+ Support site identification, qualification, activation, monitoring, and closeout activities across clinical studies.
+ Maintain Trial Master Files and essential study documents to ensure inspection readiness and regulatory compliance.
+ Partner with clinical study teams to develop, review, and manage study documentation required for trial execution.
+ Review and maintain informed consent forms, case report forms, and other study-related materials.
+ Generate study newsletters and communications to support investigator sites and cross-functional stakeholders.
+ Track and support study invoicing activities...