Jobs at Thermo Fisher Scientific

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

We have a vacancy for Associate Project Manager to join our Global Clinical Supplies Team in the EMEA region. This can be office based, hybrid, or fully homebased in a number of EMEA locations.

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).

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Role Overview
Manages full supply chain oversight for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements.. Acts as a department representative on all assigned projects and provides consultation services to clients. 

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. 
• 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. 
• Represents the department internally and externally at meetings, strategic projects and initiatives as per the business requirements. 
• Mentors and guides supports junior team members. 
• Participates in process improvement initiatives. 
• Maintains and uses existing tools while continously looking for improvement opportunities
• May participate in the bidding and/or bid defense opportunities
• Client contact for their supply chain strategy/requests/questions/concerns 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 5 (PM) 8+ (SrPM) years). Preferably eith experience of clinical supplies in a clinical trial environment.