Jana Siemann

Global leadership, management, general oversight and direction for Laboratory Logistics Service projects. Leading Laboratory Logistics Service teams and develop the right solution for the client to achieve operational excellence, delivery of rojects/programs on time, to budget, to the highest quality and in compliance with ICH-GCP and GCLP. Overall accountability for the execution of the Laboratory Logistics strategy on the project.

Lead Clinical Logistics Services teams to develop the right solution for the client Main Clinical Logistics Services face to sponsor Participation in proposal development process Lead the project such that it is completed within budget, schedule and according to contract specification Management of project budget including monthly revenue recognition, forecasting and cost management Perform strategy analysis with regards to financials, resources and technical solutions

• Overall responsibility for contracted activities in relation to clinical trial distribution - storage and distribution of clinical trials supplies • set up all client related documents for a successful supply chain dealing with all aspects of storage and distribution of supplies for international multi-site phase I-IV studies • Supporting day-to-day management of clinical programs (IVRS Specifications) •Responsible for ensuring that design, implementation and timelines of study deliverables are consis

• Overall responsibility for team success by agreeing, implementing and monitoring individual as well as team objectives and targets whilst ensuring adherence to company policies and procedures • Monitor team performance and activity • Plan and prioritize workload within the team • Performance evaluation • Coaching and mentoring • Project leader function (as described below)

• Overall responsibility for contracted activities in relation to clinical trial management. (set-up and validation of clinical software database, trial monitoring and close out, participation in and presentations at investigator, monitor and client meetings) • Responsible for ensuring that design, implementation and timelines of study deliverables are consistent with client and budget expectations • Management of global and regional studies worldwide • Responsible for set-up of trial-specific documents

• Responsible for supporting Project Leader in clinical study management • Responsible for all project management activities related to site initiation • Monitor site queries • Respond to investigator site inquiries • Coordinate activities related to investigator site assets

• Support of Project Management team • Transport organization and sample tracking • Data entry and query management • Auditing of accounts • Telephone calls • Supply orders

Mathematics and Sciences