Clinical Trials Associate (Madrid)

About the Company

I’m currently working with a CRO based in Spain for an exciting CTA role on a hybrid model.

About the Role

The idea is for the individual to transition from a CTA to a junior CPM. In this role, you would support clinical study teams with Trial Master File (TMF) management, document tracking, regulatory submissions, and general study coordination activities to ensure compliance and smooth trial execution.

Responsibilities

• Support clinical study teams with Trial Master File (TMF) management


• Document tracking


• Regulatory submissions


• General study coordination activities to ensure compliance and smooth trial execution

Qualifications

• 4-5 years as a junior - mid level CTA

Required Skills

• Smartsheet management experienc...