Clinical Development
Principal Clinical Pharmacology Specialist
Summary
Lead clinical pharmacology strategy and programmes across early- and late-stage drug development, including trial design, regulatory submissions and Health Authority interactions. Mentor colleagues and collaborate with global stakeholders.
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Opportunity summary
Pay: 847,000–1,245,100 DKK per year. Country: Denmark. Your impact begins here As Principal Clinical Pharmacology Specialist, you will lead clinical pharmacology programmes and set the clinical pharmacology strategy for early and late-stage development projects across our growing cardiometabolic portfolio.
From trial design and first-in-human dose setting to regulatory submissions, your scientific insight will shape how new drugs move through development. Your work helps turn science into treatments that create progress for people living with serious chronic diseases. What you’ll bring To thrive and succeed in this role, you will have:
- - A Master’s degree in Life Sciences, supported by a PhD or equivalent scientific expertise.
- - Expert knowledge of clinical pharmacology gained within the pharmaceutical or biotech industry.
- - A strong scientific and strategic mindset, combined with a solid understanding of clinical dosing, including first-in-human dose setting and pharmacokinetic/pharmacodynamic (PK/PD) relationships.
- - A proven track record of planning and conducting clinical trials, as well as working in cross-functional, global and dynamic environments.
- - Experience in interactions with Health Authorities.
- - A strong understanding of the business and the wider value chain1 …
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