Responsible for the successful execution of clinical trials by supporting clinical study teams, tracking clinical biospecimens, and managing internal and/or external (eTMF) to ensure inspection readiness at trial level. The CTA supports the Clinical Trial Manager and SVP of Development Operations with administrative activities.

In this CRA role, you’ll utilise your therapeutic knowledge in Oncology to oversee clinical studies. Working at the core of clinical research, you’ll be exposed to protocols and experience a dedicated partnership with your team. As a CRA you are the main sponsor representative, providing key project updates.

The Senior Clinical Research Associate (Sr. CRA) is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. The Sr.CRA works closely to ensure that study commitments are achieved efficiently.

The Global CTA performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities. Tasks include essential document collection, site recruitment, regulatory submissions and clinical data review, while maintaining study documentation in applicable systems.