Research Analyst

• Responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level.
• Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed both virtually and on site visit.
• Collaborate with the Site Manager to assure that the site complies with the protocol and is inspection ready.
• Conduct monitoring activities using different methods, (e.g., both on site and remote).
• Verifies required clinical data entered in the Case Report Form (CRF) is accurate and complete.
• Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary.

Senior Clinical Research Associate – Oncology Experience Required

Data Research Analyst – Loans

Research Analyst – German Speaking

Clinical Research Associate II