In-House Clinical Research Associate
$50K/yr – $70K/yr
Responsibilities Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, etc Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs Responds to sites’ regulatory board requests for protocol and ICF clarification as needed Ensures all required site regulatory documents and approvals

