Basel, Switzerland
Internship Explorer
Internship Explorer
Our Global Internship Programme in Innovation & Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world. Are you ready to join a global network spanning 20+ countries, where bright minds collaborate to tackle real-world challenges in Innovation & Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within? In this internship, you will support a high-impact precision safety project focused on obtaining scientific input from the European Medicines Agency (EMA) on the broader application of Roche’s Precision Safety Toolbox (PST). The project combines multi-omics, advanced human cell models and AI-based analytics to better understand, predict and mitigate safety risks at the individual patient and patient-subgroup level. By contributing to this work, you will help advance a more proactive, data-driven approach to safety management in clinical development, with the goal of improving patient outcomes and reducing the burden of toxicity. Over the first 3 months, you will support the preparation and follow-up of an EMA scientific advice meeting, including key scientific documents and implementation activities. This internship also contributes to Roche’s sustainability priorities by supporting more equitable health outcomes and promoting innovative non-animal approaches in product development. It offers a unique opportunity to gain insight into cutting-edge safety science while engaging with regulatory discussions that can shape future clinical programs. The Opportunity * Support the preparation of a comprehensive briefing document for the EMA scientific advice meeting, outlining Roche’s proposed Precision Safety Toolbox approaches * Contribute to the scientific and operational preparation of the EMA meeting together with internal cross-functional stakeholders * Participate in internal discussions to help refine key scientific questions, messages and supporting evidence * Join the EMA scientific advice meeting and contribute to the scientific discussion where appropriate * Help capture, organize and synthesize feedback received from the regulatory interaction * Support the development of a post-meeting implementation plan to translate EMA feedback into actionable next steps * Contribute to the preparation of a position paper describing how the Precision Safety Toolbox can be leveraged across clinical programs * Gain exposure to innovative approaches in precision safety, including omics, advanced in vitro models and AI-driven analytics
