Robert Kömpf

Conducted monitoring visits for six clinical studies in dermatology, oncology, and neurology. Responsible for checking and maintaining data in Medidata Rave, CTMS, Argus, and other systems.

Performed monitoring visits for two clinical studies focused on atrial fibrillation and ischemic stroke. Ensured data integrity in Medidata Rave, CTMS, Argus, and other systems.

Conducted monitoring visits for two clinical studies in lung cancer and lipoprotein (a). Responsible for data verification in Medidata Rave, CTMS, Argus, and other systems.

Managed submissions for medical device studies to Ethics Committees and health authorities. Oversaw monitoring of study sites and contributed to study document reviews.

Performed data cleaning for a PTCA study and conducted user acceptance testing for a study on intraocular capsule rings.

Managed vendor relationships for programming and translations of electronic Patient Reported Outcomes (ePRO) questionnaires. Participated in user acceptance testing for ePRO devices.

Oversaw ten investigator-initiated oncology studies, managing contracts and data exchange agreements.

Worked as a Clinical Research Scientist in major trials, focusing on endpoint tracking and data review for cardiovascular medications.

Served as primary contact for six countries in a Phase III chronic heart failure study, tracking endpoints and managing queries and patient recruitment.

Designed Oracle databases and trained end users on SQL*Forms and Clintrial systems.

Designed databases and wrote validation programs in SAS for clinical data management.

Provided support for a text retrieval system.

Completed full-time training and received a certificate in EDV-Fachmann Wirtschaft, focusing on economic data processing.

Studied biology with a focus on microbiology, alongside subsidiary subjects including genetics, biochemistry, and hygiene. Completed a diploma thesis on monoclonal antibodies at Medizinische Klinik Tübingen.