The Clinical Scientist position supports early development in the Neuroscience & Rare Disease DTA, based in Basel. Responsibilities
Support development and preparation of clinical science information for inclusion in the Clinical Development Plan. Write or amend protocol/ICF documents and construct appropriate CRFs under guidance of the Lead/Senior Clinical Scientist. Coordinate cross‑functional teams for internal and external clinical presentations and communications (investigator meetings, study site interactions, patient information, study newsletters). Present at 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, and Clinical Directors to execute the Medical Data Review Plan, interpret data, and contribute to study reporting. Act as medical monitor of Phase1 and Phase2 clinical trials in Parkinson’s and Alzheimer’s disease. Apply advanced imaging techniques to measure neurodegeneration (e.g., neuromelanin‑MRI) in Parkinson’s and Alzheimer’s disease. Contribute to Clinical Trial Application (CTA)/Ethics Committee (EC) written interactions, briefing packs, responses to Health Authority (HA) questions, and clinical science data for regulatory submissions. Qualifications
Degree in Medicine required (MD, MBBS). Advanced clinical or science degree (PhD, PharmD, MSN, MPH, etc.) highly preferred. 1 to 3 years of clinical development experience. Familiarity with governing laws, regulations, and guidelines on global clinical trial execution (GCP, ICH, FDA, EMA, etc.). Good understanding of multidisciplinary functions involved in drug development. Some therapeutic area–relevant clinical trial experience or clear potential to assimilate with support. Strong collaborative skills and ability to work effectively within a geographically distributed global team. Roche is an Equal Opportunity Employer.
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Support development and preparation of clinical science information for inclusion in the Clinical Development Plan. Write or amend protocol/ICF documents and construct appropriate CRFs under guidance of the Lead/Senior Clinical Scientist. Coordinate cross‑functional teams for internal and external clinical presentations and communications (investigator meetings, study site interactions, patient information, study newsletters). Present at 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, and Clinical Directors to execute the Medical Data Review Plan, interpret data, and contribute to study reporting. Act as medical monitor of Phase1 and Phase2 clinical trials in Parkinson’s and Alzheimer’s disease. Apply advanced imaging techniques to measure neurodegeneration (e.g., neuromelanin‑MRI) in Parkinson’s and Alzheimer’s disease. Contribute to Clinical Trial Application (CTA)/Ethics Committee (EC) written interactions, briefing packs, responses to Health Authority (HA) questions, and clinical science data for regulatory submissions. Qualifications
Degree in Medicine required (MD, MBBS). Advanced clinical or science degree (PhD, PharmD, MSN, MPH, etc.) highly preferred. 1 to 3 years of clinical development experience. Familiarity with governing laws, regulations, and guidelines on global clinical trial execution (GCP, ICH, FDA, EMA, etc.). Good understanding of multidisciplinary functions involved in drug development. Some therapeutic area–relevant clinical trial experience or clear potential to assimilate with support. Strong collaborative skills and ability to work effectively within a geographically distributed global team. Roche is an Equal Opportunity Employer.
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