National Travel Required
Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study
Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conducting the clinical study throughout the study period.
Trains investigational site staff as necessary
When applicable, supports preparation of regulatory and / or EC submissions
Apply on company website Madrid, Spain Remote (Global) Full-time
Ergomed is hiring a Clinical Research Associate II
About company
Ergomed is a global clinical research organization (CRO) delivering medicines the world can trust. The company specializes in providing custom clinical solutions across the drug development lifecycle, supporting trials in over 100 countries.
With a focus on patient-centricity and operational excellence, Ergomed offers a broad range of specialized services including clinical monitoring, regulatory affairs, biometrics, medical writing, and strategic consulting. Their Ergomed CARE™ solutions enhance trial quality by supporting both patients and investigators.
The company is committed to advancing global healthcare through a strong mission, vision, and values, backed by a team of experienced professionals driving clinical research excellence.