Clinical Scientist

Join GE HealthCare to help develop our growing team in Clinical Development. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our main responsibilities are to drive clinical strategies successfully, i.e., leading and maintaining products throughout their entire life cycle management.

We are an international team who values cultural and personal diversity in an informal, friendly, and respectful atmosphere.

Scientific group leader within enzyme assisted carbon capture and -conversion - DTU Bioengineering

We are seeking a scientific group leader with extensive experience within industrial biocatalysis. This includes a documented record for work within discovery, design, engineering, characterization, and/or application of industrial enzymes.

We expect a level of experience which corresponds to several years of post doc work with significant independence within e.g. selection of methods, scientific writing, and prioritization of research questions.

In addition to being responsible for your own research activities, you will be engaged in the supervision of graduate students, organization of the laboratory and contacts to external collaborators.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Farmaceuter til Regulatory Affairs

Vi mangler hurtigst muligt 2 Regulatory Managers med interesse for og meget gerne erfaring med Regulatory Affairs. Stillingen byder på et bredt udvalg af opgaver, og du vil også få mulighed for at arbejde med marketing compliance.

Du skal bl.a. lave compliance review af marketingaktiviteter og -materialer for den farmaceutiske industri og anmeldelser til Etisk Nævn for Lægemiddelindustrien samt oversættelser af regulatoriske og medicinske dokumenter (dansk/engelsk).