**Work Schedule**Standard (Mon-Fri)**Environmental Conditions**OfficeSupports supply chain for moderate complex global clinical trials.
Ensures project/study activities are incompliance with company and client requirements.
May act as a representative and project lead for thedepartment on less complex projects.Essential Functions- Develops study specific plans for each assigned project.- Meets with internal teams to coordinate efforts, provide recommendations andrisks, and update project reports/spreadsheets.- Ensures fluent communication and interaction between internal departments inorder to avoid obstacles during the course of the study.- Integrates all clinical supplies activities into the supply chain to support projectlogistic 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 qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to2+ years).In some cases an equivalency, consisting of a combination of appropriate education, trainingand/or directly related experience, will be considered sufficient for an individual to meet therequirements 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 decisionmaking 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