Role overview

• Supports supply chain for global clinical trials. Ensures project/study activities are in compliance with company and client requirements.

A day in the life

• 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:

• We require experience working in a clinical trial environment with clinical supplies.
• 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