**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
Supports supply chain for moderate complex general 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

📌 Associate Project Manager, Global Clinical Supplies (Latam) (Nápoles)
🏢 Thermo Fisher Scientific
📍 Nápoles