About the Company
I’m currently working with a CRO based in Madrid for someone based in Europe for exciting CTA role on a fully remote basis.
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 experience