Manages and co-ordinates all technical and service aspects of a project. This will range from initial discussions with clients, development of the project specifications, documentation aspects of setting up the project and management of all project related activities through to project/study completion.

Assessment of clinical protocol and other client supplied study specifications in conjunction with Proposals Group, FACTS Technical Group, Clinical Supplies, Operations and Procurement to help design Supply Chain solutions to meet the needs of the trial. Provision of data and technical input to the Proposals group to help them in the creation of proposals. Working with the internal stakeholders and or client to finalize logistics requirements. This may include Project meetings at the client site or at Fisher. Coordination and communication of all relevant activities, both internal and external to ensure that all services and products are ready for the start of the study or as required by the client. Overall responsibility for ensuring that activities come together in a timely manner to meet the client and study requirements. Timely provision of reports and other information to clients and internal team. Organization and delivery of training, including cross training of other members of Fisher where appropriate. Provide input into the writing and review of departmental SOP’s. Participation in client meetings / bid support meetings / teleconferences, where appropriate. Writing of documentation for the control of packaging operations Work with Scheduling to optimize the production of clinical supplies – balancing the client requirements with best use of available production capacity Support direct supervisor to oversee day to day packaging operation team to ensure all processes are compliant to quality and SOP standard. Be responsible of label printing jobs. Has no authority in making any financial decision.