Job Description

　　Summarized Purpose:

　　Supports supply chain for moderate 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 Functions

　　Develops 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 team environment, as well as work independently with moderate guidance

　　Basic understanding of clinical supply operations