Job Description
CDMX
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
The Quality Assistance1 role, supports the operational quality and documentation management of clinical trials across CDC and adjacent affiliate countries. This position ensures compliance with regulatory requirements, SOPs, and internal processes while supporting effective trial execution, quality oversight, and coordination across cross-functional teams.
**What You Will Do:**
+ **Trial Documentation & eTMF Management**
+ Oversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions.
+ Maintain and ensure compliance of the electronic Trial Master File (eTMF), including timely uploads, quality checks, and archiving at stu...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
The Quality Assistance1 role, supports the operational quality and documentation management of clinical trials across CDC and adjacent affiliate countries. This position ensures compliance with regulatory requirements, SOPs, and internal processes while supporting effective trial execution, quality oversight, and coordination across cross-functional teams.
**What You Will Do:**
+ **Trial Documentation & eTMF Management**
+ Oversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions.
+ Maintain and ensure compliance of the electronic Trial Master File (eTMF), including timely uploads, quality checks, and archiving at stu...