- Planning, coordinating and conducting international clinical trials in the region (especially Austria, Belgium, Netherlands, Portugal)- Management and review of the project status (e.g. submission to Ethic Committees and Competent Authorities, patient recruitment, clinical trial data capture, keeping timelines, study budget, etc.)- Communication and working with global and local teams, supervising monitoring activities

- Planning, coordinating and conducting international clinical trials in the country, especially in the therapeutic areas of respiratory, ophthalmology, neuroscience, transplantation and cardiology.- Management and review of the project status, e.g. Site selection and feasibility Submission to Ethic Committees and Competent Authorities Preparation of informed consents in cooperation with Clinical Research Medical Advisors Site budget monitoring and contract negotiations Supervision of patient recruitment Close collaboration with global and local teams Management and tracking of study medication Co-Monitoring

- Monitoring, co-monitoring and assistance of phase II-IV studies in the therapeutic area of rheumatology, cardiology, urology and gynecology- Submissions to Ethic Committees and Competent Authorities- Drug accountability- Data entry and data processing (data review, encoding, discrepancy tracking)- Trainer of data entry systems and SOPs (Standard Operation Procedures)- Administrative support for CRAs (clinical research associates)- Preparation in case of audits and inspections- Electronic submissions of adverse events to Merck, Inc.

- Communication with creditors, debtors and lawyers- Office management (MS Office)- Invoice processing

- Preparation and cost accounting of proposals- Preparation of minutes during proposal meetings