Clinical Researcher - Diabetes Trials & Innovation

Aarhus Universitetshospital

Aarhus

Presencial

DKK 650 000 - 900 000

Tempo integral

Há 12 dias
Gerador de candidaturas

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Resumo da oferta

Steno Diabetes Center Aarhus, based at Aarhus University Hospital, invites a clinical researcher to join the Steno Trial Unit for a 1-year, time-limited position starting 1 November 2026 or as soon as possible thereafter. The role focuses on conducting cutting-edge clinical trials in diabetes and cardiometabolic diseases under established protocols.

As a medical doctor, you will work with an multidisciplinary team performing hands-on examinations, coordinating trial logistics, data registration

Qualificações

  • MD-level physician authorized to work independently.
  • Good English communication skills, both written and verbal.
  • Analytical mindset with ability to devise innovative solutions.
  • Enthusiastic, dedicated and collaborative attitude.
  • Motivated to perform hands-on clinical examinations under protocol guidance.
  • Understanding of Good Clinical Practice (GCP) and trial protocols.
  • Ability to work independently as well as in a multidisciplinary team.

Responsabilidades

  • Recruitment of subjects to research and assist in logistics of trials.
  • Coordinate and perform clinical examinations including muscle/fat biopsies.
  • Register trial data accurately.
  • Coordinate with internal and external partners.

Conhecimentos

MD-level authorization
English proficiency
Analytical mindset
Collaborative attitude
Hands-on clinical exams
GCP knowledge
Independent & team work

Formação académica

MD degree

Descrição da oferta de emprego

Steno Diabetes Center Aarhus, based at Aarhus University Hospital, invites a clinical researcher to join the Steno Trial Unit for a 1-year, time-limited position starting 1 November 2026 or as soon as possible thereafter. The role focuses on conducting cutting-edge clinical trials in diabetes and cardiometabolic diseases under established protocols.

As a medical doctor, you will work with an multidisciplinary team performing hands-on examinations, coordinating trial logistics, data registration

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