Beatrix Muggli

Triaging incoming cases, Adverse Event Processing, Follow-up query management, monthly reconciliation Local literature review (Post-marketing, Clincial trials)

Process clinical trial safety data by triaging initial and updated safety data. Process post-marketing safety data by receiving SAE and Adverse Event (AE) reports from various source. Writing and updating Narratives Coding event terms Ensuring initial reports are sent to customers or marketing authorization holders within agreed time-lines Identify and record quality problems and bring then to the attention of a senior member

managing several small CEVA-projects as local lead Administrative support in all departments Preparation tasks for the project-teams Registration of incoming cases Handling the telephone switchboard Reception Cash handling, writing invoices Taking care of national and international visitors and guests Organization of business trips, Telephone conferences Training a new colleague in Dublin ( 08/2007)

Creation of new cosmetical Products, amelioration of existing formulations, carry on and review stabilization tests Perfume evaluation, support and assist in Up-scaling, inventory control

Taking samples during packaging process, Check of expire date and country specific in-prints Quality check of the content of the package Carry out specific parameters (PH, Densitiy etc.) Data Entry Writing and maintaining SOP’s and workinstructions