Avania’s Clinical Research Associate II (CRA II) establishes, maintains and supports clinical trials. Through the monitoring process, you will verify that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents. Further, you will ensure that the conduct of the trial follows approved protocols/amendment(s), with ISO14155 or ICH-GCP, and with applicable regulatory requirements.

 

About the role

As a CRA II at Avania, you will play a key role in supporting clinical study execution through a broad range of site monitoring activities, with a particular focus on studies in Netherlands and Germany. In this role, you will help manage site relationships across multiple projects, conducting monitoring as well as other visit types needed across the study lifecycle. This position is suited to someone with prior CRA experience who can work with a high degree of independence while remaining collaborative, flexible, and responsive to study needs. You will join a team that values practical support, strong communication, and the ability to help offload more senior colleagues by taking ownership of site-facing responsibilities.

What you'll be doing

• Conduct a range of site visits across assigned studies, with monitoring visits expected to make up the majority of the role.

• Support additional visit activities across the study lifecycle, which may include feasibility, site setup, and closeout work as needed.

• Manage responsibilities across multiple active studies, with a typical workload spanning several protocols and sites.

• Travel regularly to support sites, with site activity expected to fluctuate based on study needs and assignment mix.

• Work as a well-rounded CRA II who can contribute across different operational tasks, while also supporting a more travel-focused model when required.

• Help strengthen coverage in Germany by taking on site-facing work that enables more senior team members to focus on broader priorities.