Role at a glance
- Salary
- Not Disclosed
- Location
- Allschwil, Switzerland
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- Entry Level Initial professional experience in clinical trials, clinical supply, logistics, or a related regulated industry • Experience in coordination, administrative, operational, or client-facing roles • Project Management certification from recognized institution beneficial • Strong understanding of GMP/GxP principles and quality management systems • Strong organizational and multitasking skills with high attention to detail • Ability to coordinate multiple activities and meet timelines in a dynamic environment • Experience coordinating with teams and managing stakeholder relationships • Analytical mindset with the ability to work with data and support reporting • Proficiency in Microsoft Office tools (especially Excel and MS Project) • Experience with enterprise systems like Salesforce, GPMS, and TrackWise preferred
- Education
- Bachelor’s degree in life sciences, healthcare, supply chain, business, or a related field
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Role Summary
Supports clinical trials in a fixed-term project support role, coordinating project activities, documentation, and supply-chain operations. Works with internal teams and clients to support project execution, timely delivery, and high-quality service in a structured, regulated environment.
What You'll Do
- Coordinate project activities supporting clinical trials.
- Manage project documentation.
- Contribute to supply-chain operations.
- Coordinate with internal teams and clients to support project execution, timely delivery, and high-quality service.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor’s degree in life sciences, healthcare, supply chain, business, or a related field; initial professional experience in clinical trials, clinical supply, logistics, or a related regulated industry; experience in coordination, administrative, operational, or client-facing roles; understanding of GMP/GxP principles and quality management systems; organizational, multitasking, coordination, stakeholder, analytical, data, and reporting skills; Microsoft Office proficiency, especially Excel and MS Project; fluent English; proactive, adaptable, and quality-focused approach.
Required
- Project Management certification from a recognized institution is beneficial.
- Experience with enterprise systems like Salesforce, GPMS, and TrackWise is preferred.
- Additional languages are beneficial.
Preferred
- Project Management certification from recognized institution beneficial
- Experience with enterprise systems like Salesforce, GPMS, and TrackWise preferred
- Additional languages beneficial
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, OfficeJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join our team at Thermo Fisher Scientific and contribute to advancing clinical research in a fixed-term role. As a Project Support Associate, you will support clinical trials by coordinating project activities, managing documentation, and contributing to supply chain operations.
Working closely with internal teams and clients, you will help ensure smooth project execution, timely delivery, and high-quality service. The role focuses on project coordination, stakeholder communication, and operational support within a structured and regulated environment.
This is an entry-level position requiring relevant initial professional experience, offering an excellent opportunity to further develop expertise in clinical trials and client services.
REQUIREMENTS:
• Bachelor’s degree in life sciences, healthcare, supply chain, business, or a related field
• Initial professional experience in clinical trials, clinical supply, logistics, or a related regulated industry
• Experience in coordination, administrative, operational, or client-facing roles
• Project Management certification from recognized institution beneficial
• Strong understanding of GMP/GxP principles and quality management systems
• Strong organizational and multitasking skills with high attention to detail
• Ability to coordinate multiple activities and meet timelines in a dynamic environment
• Experience coordinating with teams and managing stakeholder relationships
• Analytical mindset with the ability to work with data and support reporting
• Proficiency in Microsoft Office tools (especially Excel and MS Project)
• Experience with enterprise systems like Salesforce, GPMS, and TrackWise preferred
• Fluent English required, additional languages beneficial
• Proactive, adaptable, and quality-focused approach
• Travel to client sites or other facilities may be required
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.