Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSupports supply chain for moderately complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects.Essential FunctionsDevelops study specific plans for each assigned project.Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.Ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study.Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.Participates in ongoing training on new regulations.Education and Experience:Bachelor's degree or equivalent and relevant formal academic/vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills and Abilities:Good English and communication skills both written and verbal.Strong interpersonal, planning, organizational, problem solving, sense of urgency, and decision making skills.Demonstrated effective leadership and team building skills.Strong working knowledge of Microsoft Office suite.Strong focus on customers and attention to detail.Ability to work in a team environment, as well as work independently with moderate guidance.Basic understanding of clinical supply operations.#J-18808-Ljbffr