PHARMACOKINETICIST, PK/PD MODELLING & SIMULATION

Are you an expert in pharmacokinetic methods? Do you have experience in drug development? We are looking for a pharmacokineticist to join our team and contribute to the success of our development projects.

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Can you see yourself in this role? We want to hear from you. Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!
Upload your CV and include a few lines about your motivation for applying. No separate cover letter is needed. We ask you not to include a photo or personal information that does not relate to your professional experience.
If you have questions or want to hear more, please feel free to contact Johan Areberg, Senior Director, +46 3083 3075 (joar@lundbeck.com). Applications must be received by 14th June 2024.
We need every brain in the game – and that includes all brains and the different perspectives we bring to the table. At Lundbeck, we embrace the uniqueness of each employee, and we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at www.lundbeck.com/global/about-us/our-commitment/diversity-and-inclusion.

EveryBrainInTheGame

This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.

You will contribute to Lundbeck research and development projects:

• Responsible for the design and data analysis/interpretation of pharmacokinetic (PK) and pharmacodynamics (PD) aspects of preclinical and clinical studies, with focus on the clinical part
• Be instrumental in the strategic design of the PK/PD plan, to ensure PK can support the plan and to ensure the selected PK/PD analyses are the best and most relevant for the overall clinical development plan.
• Represent the department in cross-functional teams, including responsibility for PK/PD input to global clinical development plans.
• Write scientific reports and prepare documents for PK/PD-related sections in Investigator Brochures, study reports, manuscripts, summaries for regulatory authorities, INDs and BLAs
• Interpret preclinical PK data to inform human dose projections.