Associate Proj Mgr Clin Supplies

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

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