Dr. Silvia Stingele

Working independently on projects as well as supporting the Regulatory Affairs Managers and Director, communication with authorities and clients, working with well-known pharmaceutical companies, gap analysis of IMPDs, specialist for the software eCTDmanager, support sponsors with orphan drug designation application and scientific advice, post marketing authorisation, product tracking after authorisation, variations, sunset clause, submissions of substantial amendments for clinical trials

For RA experience see description above. Clinical Trial Management: Working in close collaboration with the Clinical Trial Manager and CRAs, coordination of international and multi-centre clinical trials, interaction with study sites and sponsors, maintenance of trial master files, organising and attending meetings with clients, writing meeting minutes, tracking and processing of clinical trial information.

Planning and development of the PhD project, conducting experiments successfully, presenting scientific data in various occasions, teaching Master and university students, leading student projects, analysis of large scale genome and proteome data, cell culture, fluorescent microscopy, cell cycle and proliferation studies.

Biochemistry; Phosphorylation studies; Mass spectrometry; Kinase assays; Phosphorylation status of Ulk1, a gateway kinase in autophagy

Molecular Oncology; PCR based assay; Detection of insertions into the Mcl-1 promoter in CLL patients and healthy individuals

Side study: Business studies with passed exams in: Marketing, Financial accounting, Management accounting, Business management