Dipl.-Oecotroph. Silke Gerrath

After successfully completing her university studies in nutritional sciences (Diplom-Oecotrophologie) Silke Gerrath started her career in the pharmaceutical industry as a sales representatives for 2 years, then moved on into clinical research. More than 20 years of work experience in clinical research allowed her to gain profound knowledge of all clinical development phases. Her approach is to deliver her work diligently and in a timely manner. In times of high workload and the need of additional temporary resources you will benefit from her capability to adapt quickly to new project demands and from her knowledge.

Therapeutic areas

Pain Management

Neurology

Psychiatry

Immunology

Viral Infections

Monitoring

Monitoring including co-monitoring: 7 trials, phases 1-4 and NIS

Co-monitoring: 2 trials, phases 2 and 3

Regions: Germany, UK, Sweden, Hungary, Lithuania, Poland

Project management

Phase 1: 5 trials

Phase 2: 2 trials

Phase 3/3b: 5 trials

Phase 4: 2 trials

NIS: 9 NIS

Regions involved: Europe and US

Outsourcing

Clinical trials, phase 1-4 and NIS

Services outsourced: clinical conduct, data management, IVRS/IWRS, ECG-central collection and central reading services, central and specialty laboratory services, imaging services, translation and linguistic validation services

Additional Qualifications

Experience in clinical trials with controlled substances in Germany

Biomarker Operations Management

Alliance Management

Site Contracts Management