Sevgi Eminel

- Performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ICH/GCP guidelines. - Supports investigators and investigative staff in fulfilling obligations with regard to local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements.

- Support in Studies, organizing and coordinating study processes - Act as contact person for all responsible in the study (Investigator, Monitor, Sponsor, Patient) - Preparation and support of initiations, monitor visits, audits and official inspections - Preparation, organization and coordination of diagnostic material, laboratory samples and test medication - Administration and archiving of the investigator files and CRFs as well as all study-related correspondence

- Responsible for developing the primary multidiscipline laboratory of the University including equipment and device selection in the field of Pharmacology, Molecular Biology, Micro-Biology, Genetics and Histology - Supplier and Procurement Management including Quality Control - Design and setting up training programs for laboratory team - Performing courses in Pharmacology to university students - Presentation of results at internal meetings, conferences and preparation of manuscripts for publica

-Provide general supervision over the laboratory and assist in management of resource allocations and day-to-day activities - Orienting new laboratory members to the policies and regulations for their research - Assist PhD students in executing, conducting analysis and reporting results - Conduct independent scholarly research and develop new methods and protocols - Team member in clinical trials for patients with moderate to severe forms of psoriasis

- Conduct experiments in animal models, including maintaining breeding stocks, genotyping and monitoring health on a regular basis - Develop and perform genomic and molecular biological experiments in vitro and in vivo - Collaborates with researchers, external agencies and institutions to develop cooperative research initiative

- Design and perform or supervise molecular biology experiments (including sample management, sample preparation, genotyping and gene expression experiments) - Perform courses in Pharmacology to medicine students - Seek, develop and qualify new technologies, reagents and assays - Perform experiments using cell and molecular biology techniques such as RT-PCR, Western blot, immunohistochemistry, Immunofluorescence and ELISA - Perform animal experiments - Design, perform and analyze experimental data

- Working on Master Thesis - Managing animal experiments - Perform Pharmacology courses for Nursing Students.

- GCP – Good Clinical Practice - GMP – Good Manufacturing Practice - LS-PPM – Life Science Process- and Project Management - Organizing and Monitoring of Clinical Research Programs - QMB – Quality Management Officer - QS – Quality Assurance Pharma - Introduction in Regulatory Affairs and Pharmacovigilance - Overview in Data Management in Pharma

Thesis: Functions of c-Jun N-terminal kinases in neuronal apoptosis and differentiation

Thesis: The antinociceptive effects of parasympathomimetics

Thesis: Calculation of vibrational spectra of Trans-N-Benzylidenaniline