Global Clinical Trial Supply Specialist

Nestlé; Konolfingen; Presencial; CHF 110.000 - 150.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible working options

Hybrid work possibilities

Learning and development opportunities

Performance based bonus

Healthcare contribution

Employee Assistance Program

Pension plan contribution

Parental leave

Descripción de la vacante

Nestlé Nutrition & Health is seeking a Clinical Trial Specialist to ensure timely, compliant delivery of clinical study products worldwide. You will collaborate with product development, clinical research, quality, pilot plant, logistics, and external partners to support study execution and continuous process improvement.

We value hands-on trial preparation, release expertise, and proactive problem-solving. English is required; German is an asset.

Formación

• Solid food science and technology knowledge from product development, quality or application environments.
• Hands-on trial preparation, execution and release experience.
• Strong project management and cross-functional collaboration skills.
• Able to communicate clearly with diverse stakeholders.

Responsabilidades

• Deliver compliant clinical study supplies on time from requirements setup to release and shipment.
• Secure materials, labelling, product analysis and release documentation for each study.
• Coordinate across sites, factories, co-manufacturers and logistics partners to keep shipments on track.
• Design tailored study solutions including coding, packing, administration and distribution.
• Train colleagues and lead continuous improvement of processes and SOPs.
• Maintain visibility of past and current studies, anticipate reproductions and manage stock lean.

Conocimientos

Food science knowledge

Project management

Organizational skills

Cross-functional collaboration

English fluency

Descripción del empleo

Nestlé Nutrition & Health is seeking a Clinical Trial Specialist to ensure timely, compliant delivery of clinical study products worldwide. You will collaborate with product development, clinical research, quality, pilot plant, logistics, and external partners to support study execution and continuous process improvement.

We value hands-on trial preparation, release expertise, and proactive problem-solving. English is required; German is an asset.