Claudia Ose
Professorin für Medizinisches Informationsmanagement, Fliedner Fachhochschule Düsseldorf at Fliedner Fachhochschule Düsseldorf- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
-
Deutsch Native or bilingual proficiency
-
Englisch Professional working proficiency
-
Französisch Elementary proficiency
-
Arabisch Elementary proficiency
Topline Score
Bio
Credentials
-
Introduction to Data Curation for SAS Data Scientists
SASApr, 2020- Oct, 2024
Experience
-
Fliedner Fachhochschule Düsseldorf
-
Germany
-
Higher Education
-
1 - 100 Employee
-
Professorin für Medizinisches Informationsmanagement, Fliedner Fachhochschule Düsseldorf
-
Aug 2018 - Present
-
-
-
University Hospital Essen
-
Germany
-
Hospitals and Health Care
-
100 - 200 Employee
-
Senior Advisor Clinical trials
-
Aug 2019 - Present
-
-
-
-
Managing Director
-
Apr 2006 - Jul 2019
Establishment of the Center of clinical trials in the university and the German network of clinical trials Design and management of clinical trials in several indications (e.g. psychiatry, neurology, nephrology, oncology. pediatrics, surgery). Statistical analysis of these trials and report writing according ICH-E3. Team leadership for relevant clinical trials Updating SOPs Setup investigator training in the university. Lectures for investigators and trial assistants Cost accounting, acquisition of third-party funds and keeping in contact with clients Show less
-
-
-
-
Project manager
-
Sep 1994 - Apr 2006
Design, management and monitoring of clinical trials in several indications (e.g. Angiology, phlebology, epidemiology and public health, oncology, non-conventional therapies, hepatology, psychiatry, neurology, pediatrics, surgery). Statistical analysis of these trials and report writing according ICH-E3. Development of 22 Standard Operation Procedures (SOP) Design of a standardized trial protocol fitting for all clinical trial according GCP (Ose, 2001) Lectures in monitoring and in GCP at university and invited lectures for the GMDS Reviewing of publications and trial protocols Cost accounting, acquisition of third-party funds and keeping in contact with clients Show less
-
-
-
-
SAS-programmer, biometrician
-
Jul 1990 - Aug 1994
Statistical analyses of clinical trials with SAS Writing of statistical reports Design of clinical and epidemiological trials and client counseling Statistical analyses of clinical trials with SAS Writing of statistical reports Design of clinical and epidemiological trials and client counseling
-
-
Education
-
Universität Duisburg-Essen
Dr. rer. medic. -
Universität Duisburg Essen
Master of Science (M.Sc.), Master of pharmaceutical Medicine -
University Hospital of Ulm for Medical documentation
medical information management, 1,5