Principal Investigator in Drug-Drug Interaction

Lundbeck A/S, H is a leading pharmaceutical company that focuses on developing innovative treatments for brain disorders. As a Principal Scientist, you will be part of the Department of Drug Metabolism within the Non-Clinical Safety Research division.Your main responsibilities will include evaluating the drug-drug interaction risk of Lundbeck development...

About the ProjectThe project aims to investigate the pleiotropic effects of drug targets on clinical phenotypes using pharmacogenomics. We will use state-of-the-art assays and technologies to generate and analyze high-dimensional datasets, providing novel insights into personalized medicine.The successful candidate will be responsible for developing and...

Lundbeck A/S, H is a Danish pharmaceutical company that develops innovative treatments for brain disorders. As a Senior Research Scientist, you will join the Department of Drug Metabolism within the Non-Clinical Safety Research division.Your key responsibilities will involve evaluating the drug-drug interaction risk of Lundbeck development compounds,...

Do you have experience as DMPK project representative within large molecule drug discovery projects? Then you might just be the new colleague that we are looking for. We have an opening for a Principal Scientist to join Translational DMPK. The department is part of the dynamic Research organization at Lundbeck located in Copenhagen. Your new role – why is...

Job DescriptionThe Senior Quality Control Scientist will be responsible for leading Quality Control activities for biologics development, working closely with CMOs, and collaborating with cross-functional teams. This role requires strong leadership skills, technical expertise, and excellent communication abilities.Key ResponsibilitiesLead Quality Control...

Senior/Principal Medical Writing Consultants Pharma IT is hiring experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing Team In this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries. In this position, you will work on-site at the client's...

At H. Lundbeck A/S, we are seeking a skilled Principal Scientist to join our dynamic Translational DMPK department in Copenhagen.About the RoleAs a key member of our research team, you will be responsible for guiding the DMPK optimization and characterization of new compounds in our discovery programs. Your expertise in pharmacokinetic analysis of biologics...

Job DescriptionWe are seeking a Senior/Principal Medical Writing Consultant to join our team. As a key member of our Regulatory Affairs & Medical Writing Team, you will work as a consultant to support our clients in the Pharma, Biotech, and Medical Device industries.In this role, you will be responsible for writing and reviewing clinical (and nonclinical)...

Role and ResponsibilitiesThe successful candidate will be working on an ambitious project funded by the Independent Research Fund Denmark, Sapere Aude entitled: "Pleiotropic effects — from drug targets to drug actions". The project aims to investigate the interplay between naturally occurring variations in prominent drug targets and clinical phenotypes for...

Biologics Quality Control ExpertiseThe ideal candidate will have minimum 5 years of experience in the biotech or pharmaceutical industry, including experience in drug-device combination products. They will also have a good understanding of GDP/GMP guidelines and knowledge of the United States Pharmacopoeia and the European Pharmacopoeia.Your New RoleAs our...

The Department of Drug Metabolism at Lundbeck A/S, H is part of the Non-Clinical Safety Research division, focused on developing innovative treatments for brain disorders. As a Pharmaceutical Scientist, you will be responsible for evaluating the drug-drug interaction risk of Lundbeck development compounds.Your main responsibilities will include collaborating...

About H. Lundbeck A/SH. Lundbeck A/S is a global leader in the development and manufacture of innovative medicines for the treatment of brain diseases. Our goal is to make a meaningful difference in the lives of people affected by these debilitating conditions.Your New RoleAs our Senior Quality Control Scientist, you will be responsible for leading Quality...

OverviewLundbeck's CMC Biologics department is responsible for the development and production of biologics drug candidates for various diseases. We are seeking a Senior Quality Control Scientist to join our team.Your New RoleAs our Senior Quality Control Scientist, you will be the technical lead and subject matter expert for Quality Control activities with a...

About UsC. H. Lundbeck A/S is a leading global pharmaceutical company that has been active in the production of drugs for more than 70 years. Our main goal is to develop and commercialize treatments for brain diseases. We are committed to delivering innovative treatments to patients around the world.Job DescriptionWe are seeking a highly skilled Senior...

Clinical Documents SpecialistWe are looking for a skilled Clinical Documents Specialist to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will be responsible for writing and reviewing clinical and nonclinical documents for regulatory submissions in the EU and US, including Module 2.5, 2.7, 2.4, 2.6, integrated summaries of...

Regulatory Affairs Document SpecialistWe are seeking a highly skilled Regulatory Affairs Document Specialist to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will be responsible for writing and reviewing clinical and nonclinical documents for regulatory submissions in the EU and US, including Module 2.5, 2.7, 2.4, 2.6,...

Clinical Documentation SpecialistWe are looking for a skilled Clinical Documentation Specialist to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will be responsible for writing and reviewing clinical and nonclinical documents for regulatory submissions in the EU and US, including Module 2.5, 2.7, 2.4, 2.6, integrated...

Job DescriptionAs a Principal Insights Strategist at GetWhy, you will be responsible for driving the adoption of our product into the workflows of insights and marketing teams in top consumer brands. Your expertise will help bridge the gap between companies and consumers, creating a deeper understanding of human experiences on a global scale.Your...

We are seeking a candidate to fill a fully funded PhD position for a period of 3 years in the Insect-Microbe Interactions research group led by Nicolai V. Meyling at the The Department of Plant and Environmental Sciences, University of Copenhagen, Denmark.Start date is 1 September 2025 or as soon as possible thereafter.The project The PhD project will form...

Medical Writing Expert ConsultantWe are seeking an experienced Medical Writing Expert Consultant to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will work as a consultant to support our clients in the pharmaceutical, biotechnology, and medical device industries. You will be responsible for writing and reviewing clinical...