Global Clinical Trial Specialist — Flexible & Impactful

Nestle SA; Konolfingen; On-site; CHF 90,000 - 130,000; Full time

Benefits offered by this job

Flexible work options

Paid holidays

Learning & development

Performance bonus

Healthcare contribution

Pension plan

Parental leave

Employee discounts

Job summary

Nestlé Nutrition & Health in Konolfingen, Switzerland, is seeking a Clinical Trial Specialist to ensure clinical study products are delivered on time and in full compliance, from production through release and shipment to sites worldwide. You’ll collaborate with product development, clinical project management, clinical research, quality, pilot plant and logistics teams.

With English fluency and a proactive approach, you will drive materials, labeling, release documentation, and cross-site

Qualifications

• Solid food science and technology knowledge from product development, quality or application environments.
• Hands-on expertise in trial preparation, execution and release.
• Strong project management skills and ability to coordinate across teams.
• Excellent collaboration and interpersonal skills, with ability to connect diverse stakeholders.

Responsibilities

• Delivering compliant clinical study supplies on time, from requirements setup through release and shipment.
• Securing materials, labeling, product analysis and release documentation that meet study specs.
• Orchestrating collaboration across sites, factories, co-manufacturers and logistics partners.
• Designing tailored solutions for studies, including coding, packing, administration and distribution.
• Training colleagues and leading continuous improvement of processes and SOPs.
• Maintaining visibility of past and current studies, managing stock and samples.

Skills

Food science & technology

Trial preparation & release

Cross-functional collaboration

Project management

English fluency

Job description

Nestlé Nutrition & Health in Konolfingen, Switzerland, is seeking a Clinical Trial Specialist to ensure clinical study products are delivered on time and in full compliance, from production through release and shipment to sites worldwide. You’ll collaborate with product development, clinical project management, clinical research, quality, pilot plant and logistics teams.

With English fluency and a proactive approach, you will drive materials, labeling, release documentation, and cross-site