In Vivo Pharmacology Technician – Large Animal Studies

Novo Nordisk; Ganløse; On-site; DKK 500,000 - 734,000; Full time

Job summary

Novo Nordisk is seeking an Advanced Laboratory Technician in Ganløse, Denmark, to lead in vivo pharmacology studies, primarily in large animals. You will work with scientists to deliver high-quality experimental outcomes supporting obesity, diabetes and cardiovascular disease drug discovery.

You will join a collaborative team, plan studies, document procedures, and ensure ethical standards. The role is based in Ganløse with some meetings in Måløv.

Qualifications

• We are seeking a Laboratory Technician with hands-on in vivo studies experience.
• Experience handling experimental data and study documentation is required.
• Familiarity with electronic laboratory documentation systems is preferred.
• Strong collaboration and communication skills across disciplines are essential.
• Experience with large animal models is an advantage.

Responsibilities

• Plan, conduct and report preclinical pharmacology studies, primarily in large animal models.
• Perform in vivo procedures including dosing, blood sampling, tissue collection and surgeries.
• Generate high-quality data and documentation to support decisions across projects.
• Collaborate with scientists and technicians to plan and execute studies.
• Maintain accurate study records using electronic laboratory systems.
• Contribute to a safe, efficient, and continuously improving lab environment.

Skills

In vivo studies

Large animal models

Data handling

Collaboration & communication

Electronic lab notebooks

Education

Laboratory Technician degree or similar qualification within biomedical sciences, pharmacology or a related field

Job description

Novo Nordisk is seeking an Advanced Laboratory Technician in Ganløse, Denmark, to lead in vivo pharmacology studies, primarily in large animals. You will work with scientists to deliver high-quality experimental outcomes supporting obesity, diabetes and cardiovascular disease drug discovery.

You will join a collaborative team, plan studies, document procedures, and ensure ethical standards. The role is based in Ganløse with some meetings in Måløv.