At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
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.
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.
Please note that this is a temporary position with a 2-year duration.
You hold a University degree (BSc, MSc or PhD) in Life Sciences, Pharmacology, Biochemistry, or a related field.
You have proven project or study management experience within drug discovery, DMPK, or related R&D functions. You have a good understanding of in vitro ADME assays, PK studies and their role in drug discovery.
You bring experience managing outsourced studies and external research partnerships (CROs).
You have the interest and capability to collaborate with technical experts in developing and maintaining study tracking or data management tools.
You bring strong interpersonal and communication skills with a collaborative, solution-oriented mindset.
You can manage multiple projects and priorities effectively, while maintaining attention to detail.
Unwavering focus, collaborative teamwork and exceptional delivery are key behaviours that drive our mission of doing now what patients need next. Together, we can be transformative.
If you are passionate about contributing to a committed team and have the dedication to partnership and innovation, Roche is the place for you!
Every role at Roche plays a part in making a difference in patients’ lives.
Apply now and join us in making an impact!
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.