ADME Pharmacokinetic Study Manager (Temporary for 2 years)

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The Position

In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.

At pRED, we are united by our mission to transform science into medicine.

Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.

pRED’s Pharmaceutical Sciences (PS) group enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.

PS supports discovery and development across the whole value chain from target assessment to on-market.

As part of the Translational Safety Assessment Chapter in Pharmaceutical Sciences, you will play a key role in accelerating drug discovery by ensuring the efficient delivery and quality of in vitro ADME screening data and in vivo PK screening.

The Opportunity

We are looking for an experienced and highly motivated ADME Screening & Pharmacokinetic  (PK) Study Manager to manage outsourced in vitro and in vivo studies, coordinate automated study requests and tracking, and collaborate with both internal experts and external partners to continuously improve our scientific and operational excellence.



* You support the outsourcing and coordination of in vitro ADME screening assays and PK studies, ensuring operational efficiency and timely data delivery.


* You work with automated study request systems and tracking workflows, supporting transparent and efficient study management.


* You partner with scientific experts, project teams, and contract research organisations (CROs) to optimise assay performance and resource allocation.


* You develop and maintain study tracking tools and contribute to process automation initiatives that enhance data visibility and efficiency.


* You communicate study progress, timelines and outcomes clearly to stakeholders, ensuring alignment across functions.


* You foster a collaborative environment and contribute to continuous improvement in screening operations and partner management.

Please note that this is a temporary position with a 2-year duration.

Who you are



* You hold a University degree (BSc, MSc or PhD) in Life Sciences, Pharmacology, ...