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