Senior Clinical Neuro Scientist

Gi Group (United Kingdom); Basel; On-site; CHF 140,000 - 190,000; Full time

Job summary

Hoffmann La-Roche in Basel is seeking a senior Clinical Scientist with extensive experience in neurological indications such as Multiple Sclerosis and Alzheimer's Disease. You will develop and write essential study documentation and provide scientific input to regulatory and operational documents.

You will oversee ongoing monitoring of clinical activities, data collection, review, analysis and interpretation, and present results for informed decision-making.

Qualifications

• Requires PhD or Masters with extensive clinical scientist experience.
• 5+ years in the clinical scientist role across neurological indications (MS, AD).
• Strong analytical and quantitative data review, analysis, and reporting skills.
• Solid understanding of phase 2-3 clinical development, study design, and international guidelines.
• Collaborative, solution-oriented, able to make independent decisions.

Responsibilities

• Develop and write study documentation: protocols, informed consent forms, and clinical study reports.
• Monitor ongoing clinical activities, data collection, data review and interpretation; present results for decision-making.
• Main point of contact for data management related to periodic reviews and data cleaning.
• Participate in SMT study management to meet trial deliverables within timelines, budget, and quality standards.
• Provide training and science input to operations staff and study sites as agreed with clinical operations.
• Monitor study progress and investigate issues affecting results or completion; apply problem-solving strategies.
• Bring a proactive, energetic mindset and contribute to interdisciplinary clinical project teams.

Skills

Clinical scientist

Neurology

Data analysis

Study management

Regulatory knowledge

Education

PhD or Masters with extensive clinical scientists experience

Job description

For Our Client, Hoffmann La-Roche, we are searching for a senior Clinical Scientist, experienced in neurological indications such as Multiple Sclerosis and Alzheimers Disease.

Tasks & Responsibilities:

• Your activities will include the development and writing of study documentation including protocols, informed consent forms, clinical study reports, as well as clinical science input for study-specific operational and regulatory documents.
• You will be responsible for ongoing monitoring of clinical activities and study conduct, coordination of data collection, data review, analysis, and interpretation as well as preparation and presentation of results for informed decision-making.
• You will be the main point of contact for data management regarding periodic clinical data review and data cleaning
• You will participate in study management, as clinical science representative, to ensure trial deliverables are met according to timelines, budget, quality standards and operational procedures, within a global multidisciplinary cross-functional Study Management Team (SMT)
• You will provide training and science input to operation colleagues and study site staff, as agreed with clinical operations
• You will monitor study progress on a regular basis to identify any problems or issues that could affect the results or completion of the study; you will investigate and employ problem-solving strategies.
• You should bring a positive, energetic, responsible, creative, curious and solution-seeking mindset and proactively contribute to interdisciplinary clinical project teams with integrity, passion and courage.

Must Haves:

• PhD or Masters with extensive work experience as a clinical scientists
• 5+ years the clinical scientist role in different neurological indications, preference for Multiple Sclerosis and Alzheimer’s Disease
• You possess strong analytical and quantitative skills, with a proven track record in clinical data review, analysis, and reporting data.
• You have a solid understanding of clinical development processes (phase 2-3), study design principles, and international clinical research and safety guidelines.
• You are a collaborative, solution-oriented scientist who communicates effectively across teams, values diverse perspectives, and makes sound, independent decisions.
• You have excellent written, oral communication, and presentation skills.