Dr. Karolina Can

-Trainee in the field of Clinical Trails in Project Management Early Phase -Initiation and support of Phase I Clinical Trials (preparation, drafting, and submission of clinical trials documents to Regulatory Authorities (BfArM/PEI) and Independent Ethics Committees -Study compilation based on SOPs and source data documentation such ICSF and TMF -Assistence in sponsor meetings such as Site Initiation Visit -Pre-audit activities

-Quality management and conduct of multiple in pre-clinical research projects with a keen attention to details and under time pressure -Implementation of scientific questions into projcts through maintenance of project troubleshooting and lessons learned -Supervision of interdisciplinary project of PhD colleagues with a hand on their doctoral thesis

Bench Work, Neurophysiology, Microscopy, Bioinformatics, Extensive database and statistics, Proved planned and experiments designig Problem solving and troubleshooting, Scientific reports writing, Professional data presentations, Supervision of medicine students, lab teaching

Primary cell culture, Immunostaining, DNA & RNA isolation, Western Blot, Gel electrophoresis, SDS-PAGE, PCR, qRT-PCR, GenomeWalking, Protein isolation & purification, Trizol method, Sequencing, Spectrophotometry, Bioinformatics

Extensive knowledge gained from the field of Biology & Genetics. Master thesis proceeded on genetic disorder Rett syndrome, and combined with extended aspects of neuroscience at Georg-August-Univertität Göttingen, Germany.