Martina Semmel

Leads DM activities for assigned study; organize, monitor and track data cleaning, data review, query management, and database lock; generate study metrics and status reports; represent DM at Clinical Trial Team meetings; insourcing/outsourcing partners’ management; ensures DM assigned to study have required training; ensure SDTM deliverables, perform and/or coordinates QC

• Providing overall leadership / management for programming, data integration, data processing • Accountability for the execution of the Data Operations strategy and the Data Operations’ Technology • Coordination of the Data Operations team members and their activities across all geographies • Ability to work within project and/or across therapeutic areas including Infectious Diseases, Oncology, Cardiovascular, CNS etc. • Vendor management experience – primary study contact

Clinical Data Manager in infectious diseases department, qc of CROs

Klinische Studienkoordinatorin, Regulatory Affairs, Übersetzungen

Data Management, Anlegen und Führen von Datenbanken in SAS, Einweisung und Überwachung von Dateneingebern, Schulungen von Monitoren, CRF-Erstellung, CRF-Programmieren in Access