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