Beate Rohde | Head Development Clinical Pharmacology
Bayer Pharma

2005 Board certification as Clinical Pharmacologist Professional Experience (incl. Memberships) 1992 - 1993 Internship (Internal Medicine) 1993 - 1995 Scientist, Clinical Pharmacology, University of Rostock 1995 - 2001 Scientist, Clinical Pharmacology, Schering AG, Berlin Fields of responsibility: - Clinical Pharmacology Lead responsible for several early/ late development projects (e.g. antihormones, stroke, pulmonary hypertension) - Study Manager, Investigator in many phase I studies 2001 - 2003 Head of Monitoring and CRO-Management, Clinical Pharmacology, Schering AG, Berlin Fields of responsibility: - Clinical Pharmacology Lead in development projects (e.g. contraception, menopause management) - Head of CRA group, built up of CRO Management within CP 2003 – 2005 Head of Study Management, Clinical Pharmacology, Schering AG Fields of responsibility: - Pharmacodynamic Expertise / Study Management for all early development projects within therapeutic areas Womens Healthcare (WH), Diagnostic Imaging (DI) and Specialized Therapeutics (STH) - Medical Expertise for ClinPharm studies / Study Management within late-stage development projects 2005 - 2010 Head of Clinical Pharmacodynamics (WH/DI/STH), Clinical Pharmacology Schering AG and Bayer Schering Pharma AG, Berlin Fields of responsibility: - Pharmacodynamic/Medical Expertise for all early development projects within therapeutic areas WH, DI, STH including an inhouse investigational CP- Unit - Pharmacodynamic/Medical Expertise for ClinPharm part during late-stage development projects