Clinical Scientist - Late Stage Development

Job description

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. The PositionThe OpportunityAs a Clinical Scientist - Late Stage Development, you will support our cross-functional molecule and study teams in executing clinical strategies and Phase 2-3 clinical trials to deliver medically differentiated therapies for patients. Working closely with experienced Clinical Scientists and Medical Directors, you will contribute directly to study documentation, medical data reviews, and regulatory submissions. Contribute to the preparation and writing of Clinical Development Plans (CDPs), protocols, informed consent forms (ICFs), and Case Report Forms (CRFs). Conduct ongoing medical and safety data reviews to ensure accurate data interpretation and support study reporting. Support clinical trial application (CTA) submissions, briefing packs, and written responses to Health Authority inquiries. Collaborate with study site personnel to optimize trial conduct and resolve clinical queries effectively. Present study updates and clinical science insights at internal cross-functional meetings, investigator meetings, and scientific events. Assist in drafting abstracts, posters, and presentation materials for external scientific conferences. Who You Are You are a detail-oriented, curious life science professional eager to grow your career within clinical drug development. You thrive in collaborative, cross-functional environments and are passionate about translating scientific insights into meaningful health solutions. Bachelor’s degree in Life Sciences required; an advanced degree (e.g., PhD, PharmD, Master’s in Life Sciences or Public Health) is strongly preferred. Basic understanding of global clinical trial execution, including GCP (Good Clinical Practice) and regulatory frameworks (e.g., ICH, FDA, EMA). Broad foundational knowledge of multidisciplinary functions involved in drug development. Strong written and verbal communication skills, with the ability to summarize complex clinical information clearly. Collaborative mindset with demonstrated ability to contribute effectively within dynamic team settings. How to Apply Ready to join our team? Please submit the following documents: Updated CV, Cover Letter, Copy of your Higher Education Diploma Who we areA 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.