General Management, Project Management, Clinical Outsourcing, Contract- and Vendormanagement

General outsourcing and project management activities, mainly phase I and II in an oncology setting, contracting, and compiling of subsidiary arrangements (transfer of obligation, quality agreement, SCC, etc.).

General project management set-up, conduct and close-out activities, Project oversight as Project Director for global studies. Vendor management and performance evaluation

Responsibilities for the construction, negotiation and ongoing management of global contracts with
Clinical Research Organizations (CROs), third-party vendors (Data Management, IVRS, Central
ECG/Spirometry, Central Labs, Consultants, Health Care Professionals, etc.) and other providers as
necessary for the successful execution of global clinical trials and pharmaceutical research endeavors.
Member of  the Board of Saving generating from outsourcing activities.

Outsourcing activities with focus on budget consolidation, change order negotiation and contract execution.

Full responsibility for the integration of Progenitor International Research and Encorium Inc.

Founder and Managing Director - Progenitor International Research AG, Baar, Switzerland
Provided executive level oversight and management of all activities of Progenitor International
Research in Latin America, India and Far East. Vaccine focussed CRO:

• Global project oversight for a 23.000 Patients vaccine study in LATAM for global big Pharma
• Project Responsibility for eight vaccine studies in PR China
• Consulting Crucell/Berna Biotech in four vaccine projects
• Consulting Merkle/Ratiopharm in BA/BE studies in India

Responsible for operational activities, Developing and implementing a strategic business plan to build
up a Clinical Research Organization in accordance with all legal and regulatory requirements.

Germany and Basel, Switzerland

Monitored international clinical trials in accordance with GCP, guidelines and company's SOPs.

Responsibilities included the construction, negotiation and ongoing management of global contracts with Clinical Research Organizations (CROs), third-party vendors (data management service providers, central ECG-reading providers, laboratory service providers, and consultants) and other providers as necessary for the successful execution of global clinical trials and pharmaceutical research endeavors

Germany

From To Business Position

Founder, Owner and Managing Director of a pharmaceutical development and marketing company for
blood plasma derived pharmaceuticals. Chief Scientific Officier for Regulatory, Medical Information and Development.