Annette Burggraf

Travelled in Asia, Europe, US and Cuba

- responsible for local protocol and site feasibility assessment and ensuring adequate site selection - planed, executed, managed and reported Amgen sponsored studies and was responsible for timeliness and quality of study deliverables in accordance with SOPs, ICH/GCP Guidelines and local regulations - single point of contact at a Project Level for local staff and global study management

- managed Phase I-III oncological ophthalmological and medical device Trials in Switzerland, Germany and United Kingdom - Marketing experience in representing Appletree at the annual congress at ARVO (Association for Research in Vision and Ophthalmology) - produced, maintained and adhered to Project budgets

- prepared and submitted study dossier to Swissmedic and Ethics Committees in Switzerland for a study in CNS - conducted feasibility studies in Switzerland and Germany - data cleaning

- managed processes required to scan, evaluate and report on Images taken for clinical studies - train radiologists and other site staff on Phase I-III studies

- selected, initiated, monitored and closed out sites - compiled documents for regulatory submissions in the UK - wrote protocol and amendment for Phase II Trial in hepatocellular cancer - selected CRO and central laboratory - organised and conducted Investigator Meeting in Hong Kong - devised communication plan, monitoring guidelines, project plan, CRFs, gave input to data specifications - conducted data cleaning and data base lock produced annual safety Report for the programme

teaching Chemistry, Biology and Physics to Ages 11-18

Chemistry

Languages: Latin, English and French, later German and Chemistry