Senior ADME Scientist - DDI & Drug Disposition

Novo Nordisk A/S; Denmark; Remote; DKK 743,000 - 1,092,000; Full time

Job summary

Novo Nordisk A/S in Denmark seeks a Principal ADME Scientist to lead evaluation of ADME and DDI risks across late-stage discovery and development toward regulatory submission. You will provide scientific leadership, support key project decisions, and shape strategies for ADME- and DDI-related questions across modalities.

You will design and interpret in vitro/in vivo studies, guide complex study designs, interact with regulatory authorities, mentor junior scientists, and champion innovations to

Qualifications

• Ph.D. is preferred or Master’s degree within pharmaceutical or medical sciences or equivalent area.
• Several years of relevant experience within ADME and ideally DDI in drug development.
• Solid experience with ADME and DDI study conduct.
• Demonstrated knowledge of interpretation of ADME/DDI results.
• Strong communication and stakeholder management skills.

Responsibilities

• Design, conduct, and interpret in vitro and in vivo ADME/DDI studies across modalities.
• Inform and guide projects on ADME- and DDI topics.
• Interact with regulatory authorities and contribute to regulatory documents.
• Champion innovation and new scientific initiatives in development programs.
• Translate results into actionable project decisions and strategy.
• Mentor junior scientists and share knowledge within the team.

Skills

ADME/DDI experience

Education: PhD/MS

Bioanalytical MS

Study design

Regulatory support

Project leadership

Due diligence

Communication

Mentoring

Education

PhD or Master in pharma/medical sciences

Tools

Mass spectrometry

Job description

Novo Nordisk A/S in Denmark seeks a Principal ADME Scientist to lead evaluation of ADME and DDI risks across late-stage discovery and development toward regulatory submission. You will provide scientific leadership, support key project decisions, and shape strategies for ADME- and DDI-related questions across modalities.

You will design and interpret in vitro/in vivo studies, guide complex study designs, interact with regulatory authorities, mentor junior scientists, and champion innovations to