The Opportunity As 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.
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.
