• Disciplines include In Vivo, Pharmacokinetics, Clinical and Whole Body Autoradiography studies. I work with Study Directors in analysing data, responding to QA audits on regulatory projects, highlighting any anomaly’s and am responsible for peer reviews on study documents. I am also the primary coordinator for a new business in fast Pharmacokinetics.• I maintain study schedules in line with internal and external client expectations and review study compliance against protocols, SOP’s and regulatory guidelines. I am also responsible for compilation of study protocols and reports. I am responsible for pre-initiation and other study related meetings and communicate with study teams to ensure milestones are met. I serve as a primary contact with internal and external clients as required and deputise in the absence of Study Directors.• Working with department managers I am responsible for ensuring all study amendments are passed for costing across the department, with sound knowledge of the financial aspects of our business with respect to study costs. I hold 2 years’ experience at Covance as a revenue specialist.• As required I am responsible for training new starters and as part of a team have prepared training documentation for the group, along with continuous process improvement.• I am currently involved in a global project requiring implementation and training of Documentum across all local Covance operational businesses.