Analytical Project Manager

Eurofins; Breda; On-site; EUR 70,000 - 100,000; Full time

Job summary

Eurofins Central Laboratory in Breda, Netherlands, seeks an Analytical Project Manager to oversee biomarker studies within clinical trials, ensuring GMP/GCP compliance and client satisfaction.

You will define milestones, manage budgets, coordinate with sponsors and audits, and sustain strong internal and external relationships through clear communication and a proactive, energetic approach.

Qualifications

• Master’s degree in Biochemistry/Life Sciences or Bachelor degree with significant industry experience.
• GxP/GLP regulatory experience.
• Biomarker experience in CRO or pharmaceutical settings.
• Strong customer focus and communication abilities.

Responsibilities

• Manage biomarker studies in clinical trials according to regulatory requirements.
• Provide operational input into quotes/proposals to align capabilities with client needs.
• Define project milestones and monitor performance from contract to invoice.
• Ensure studies adhere to global standards and budget responsibilities.
• Complete study files for regulatory inspections and support sponsor/audit activities.

Skills

Bioanalytical skills

Customer focus

Communication skills

Interpersonal skills

Relationship management

Flexible work ethic

Education

Master’s degree in Biochemistry/Life Sciences

Bachelor degree in Biochemistry/Life sciences with significant industry experience

Job description

Company 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.

Analytical Project Manager

Job Description

• 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.

Qualifications

• 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.

Additional Information

Do you meet the above profile and are you interested in an informal and pleasant working environment?