Monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all necessary activities required to set up and monitor a study. Work with 2-3 protocols and support Project Managers with trials that are larger in scope, while interacting directly with clients.
The CRA II assists in the execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This position works with confidential patient and company data and interfaces with a variety of internal and external stakeholders. To meet the needs of the Business, we are prioritizing individuals who currently reside in the Midwest or South-Central Regions, including Chicago, Dallas, Austin, Houston, or similar).
Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all necessary activities required to set up and monitor a study. Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.