Dr. Beata Bekei

Perform regular site monitoring visits in accordance with contracted scope of work, national, inernational regulations and good clinical practice. Maintaining general support and general contact with study sites. Source data verification, drug accountability

in-hause and on-site monitor activities. Source document verification process. Conduction of selection, initiation, monitoring and close-out visits. Drug accountability and reconciliation. Management of protocol deviations and violations. Contact management

Technology development in nuclear magnetic resonance technique, experimental design at cellular and molecular level, result assessment, representation at national and international conferences.

Crystal-glass transitions of high-intensity discharge lamps. Evaluation of operating failures, system/process development, experimental design.

Objectives, endpoints, design and management of clinical trials. National, international regulations, ICH-CGP, FDA, EMEA requirements. Source document verification process

Doctoral project on Parkinson´s disease and on the molecular basis of other neurodegenerative diseases.

Work on organotypic cell cultures in relation to the HPA (Hypothalamic-pituitary gland- adrenal) axis.Attain knowledge in tissue culture and cell biology techniques. Develop scientific understanding, scientific writing skills

Attain knowledge in molecular biology techniques. Diploma work on intrinsically disordered plant proteins.

Bioprocess engineering and process development. Cell and organism engineering, cloning techniques. Fermentation, enzymology and biotransformation