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Analytical Project Manager

Eurofins

Breda, NB, Netherlands permanent

Posted: April 2, 2026

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Quick Summary

The job involves managing a team of analytical professionals to analyze data and provide insights to support clinical trials in a fast-paced and dynamic environment.

Job Description

Eurofins Central Laboratory is a dynamic, global organization fully dedicated to providing global central laboratory services to support all phases of clinical trials. At Eurofins Central Laboratory, we are BOLD. We go beyond the expected. Since we are purely a central laboratory, there are no distractions allowing us to remain laser focused on the best science, technology and people.

We are part of one of the world’s leading laboratory organizations Eurofins Scientific, therefore we offer end-to-end testing solutions which are unsurpassed in the industry. Eurofins Central Laboratory is setting new standards with GLP capabilities embedded within our Central Laboratory. We support our customers with laboratory facilities in the USA, Europe, Singapore and China, and a back office in India.

For our division Eurofins Central Laboratory in Breda we are looking for a

                                 Analytical Project Manager 

 

 

• You are responsible for managing biomarker studies as part of clinical trials according to the regulatory requirements;
• You carry out consultations and provide operational input into quotes/proposals to ensure capabilities and client needs are aligned;
• You check the scope of work and budget accurately to achieve client expectations at all times;
• You define project milestones and check project performance against protocol, from signed contract to invoice paid;
• You control if the project is conducted in accordance with set global standards and procedures;
• You control the budget of assigned studies;
• You complete and accurate study files to pass prevailing regulatory inspections;
• You support sponsor and internal audits.

• You have at least a Master’s degree in Biochemistry/ Life Sciences or a Bachelor degree in Biochemistry/Life sciences along with significant industry experience;
• You have experience with G(C)LP;
• You have a relevant regulatory biomarker experience with a CRO or pharmaceutical company;
• You have a strong customer focus;
• You have bioanalytical skills.
• You have excellent communication and interpersonal skills;
• You are good at establishing and maintaining internal and external relationships;
• You are energetic and enthusiastic with a flexible and dynamic work ethic;
• You have an excellent command of Dutch and English, spoken and written.

 

Do you meet the above profile and are you interested in an informal and pleasant working environment? We are looking forward to receive your CV and motivation letter. 

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