Clinical Scientist - Ocrelizumab Clinical Science, Basel

Position Overview

Since its approval ten years ago, ocrelizumab has established itself as a standard of care for relapsing and progressive forms of Multiple Sclerosis (MS). Our work continues to improve patient experience and expand access. We are seeking a Clinical Scientist to join our global team based in Basel, Welwyn and the US. This role will support our latest development priorities within a dedicated, collaborative team focused on lifecycle innovations that impact the MS community.Responsibilities

Provide support in developing and/or preparing clinical science information for inclusion into the Clinical Development Plan. Assist in writing or amending protocol/ICF, construct appropriate CRFs, and coordinate cross‑functionally. Contribute to internal and external clinical presentations and communications (e.g., investigator meetings, study site interactions, patient information, study newsletters).Present at appropriate internal meetings, such as the Study Leadership Team. Contribute to abstracts, posters, and content for scientific meetings. Work with Lead/Senior Clinical Scientists, Medical Directors, Clinical Directors, and cross‑functional groups to execute the Medical Data Review Plan, data interpretation, and contribute to study reporting.With guidance, contribute to Clinical Trial Application (CTA)/Ethics Committee (EC) written interactions, briefing packs, written responses to Health Authority (HA) questions, clinical science data/preparations for HA interactions, and clinical data input to regulatory submissions. Qualifications

Bachelor’s Degree required (life sciences preferred). Advanced Clinical/Science Degree highly preferred (e.g., PhD, PharmD, MSN, MPH, etc.). 0 to 3 years of clinical development experience; strong potential, motivation, and willingness to learn. Familiarity with governing laws, regulations, and guidelines on global clinical trial execution; knowledge of medical aspects of GCP, ICH, FDA, EMA, and other relevant guidelines and regulations.Good understanding of the multidisciplinary functions involved in drug development. Some therapeutic area relevant clinical trial experience or clear potential to assimilate with support. Strong collaborative skills with the ability to work effectively within a geographically distributed global team.Equal Opportunity Employer

Roche is an Equal Opportunity Employer.

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