Do you have Drug Metabolism and Pharmacokinetic (DMPK) expertise with a background in medicinal chemistry, pharmacy, pharmaceutical science and/or drug discovery, and would you like to apply your expertise in a global company that follows the science and turns ideas into life-changing medicines? Then you could be the new colleague we are looking for!
We are now looking for an experienced and driven individual to join the team as a
Preclinical DMPK Project Lead
preferably with experience across multiple modalities (Senior Scientist/Associate Principal Scientist, depending on your level of professional experience). The position is placed at AstraZeneca’s dynamic R&D site in
Gothenburg, Sweden
, a world-class facility with state-of-the-art laboratories and shared spaces to accelerate decision making and problem solving while benefiting from the Swedish focus on work-life balance. The working language is English, and the site is a multicultural environment with scientists from over 70 countries.
What you’ll do:
You will work collaboratively with discovery project representatives from other disciplines including medicinal chemistry, biology, safety and pharmaceutical sciences. You will influence drug design and optimization of ADMET (absorption, distribution, metabolism, excretion, toxicity) properties. It is your responsibility to ensure delivery of all DMPK related activities, including in vitro ADME, biotransformation, bioanalysis, preclinical PK and PD underpinning human dose prediction to early drug projects from target selection to candidate drug selection. We believe that you have a solid understanding of DMPK and chemistry and that you will be able to provide expert advice and interpretation of complex drug discovery data.
Main Duties and Responsibilities will include:
Responsible for leading all DMPK related activities, including coordinating and engaging with internal and external DMPK colleagues and collaborators, on project related activities
Deliver DMPK input and data to projects within agreed timelines and to the right quality to ensure that DMPK challenges are thoroughly assessed and resolved
Contribute to the design of preclinical in vivo studies to answer crucial project questions
Accountable, together with other functions such as Medicinal Chemistry, Bioscience and Safety, for compound design and effective cross-discipline optimization
Apply an understanding of DMPK and PKPD (PK/Pharmadynamics) to support/influence project progression and strategy as well as providing the framework for human dose predictions
Prepare clear presentations related to the above for internal governance interactions