Senior Clinical Neuro-Scientist

Gi Life Sciences Basel; Basel; On-site; CHF 110,000 - 170,000; Full time

Benefits offered by this job

Veeva experience

Job summary

Gi Life Sciences Basel seeks a Senior Clinical Neuro-Scientist to provide scientific leadership for neurological trials, including Multiple Sclerosis and Alzheimer's Disease, located in Basel. You will develop study documentation and oversee data review, analysis and interpretation to support informed decisions.

You will monitor trial conduct, coordinate data management, and participate in global study management teams to ensure timely, high-quality deliverables.

Qualifications

• PhD or Master's with extensive clinical-science experience.
• 5+ years in the clinical scientist role in neurological indications (MS/AD).
• Strong analytical and quantitative skills with data review, analysis and reporting.
• Solid understanding of phase 2-3 development, study design principles and global guidelines.
• Collaborative, solution-oriented with effective cross-team communication.
• Excellent written, oral communication and presentation skills.
• Fluency in English.

Responsibilities

• Develop and write study documentation including protocols, informed consent forms and clinical study reports.
• Monitor clinical activities and study conduct, coordinate data collection, review and interpretation.
• Be the main contact for data management regarding periodic data review and cleaning.
• Participate in study management to ensure trial deliverables meet timelines, budget and quality standards.
• Provide training and science input to operation colleagues and study site staff.
• Monitor study progress to identify problems and implement solutions.

Skills

Analytical skills

Data analysis

Communication skills

English fluency

Education

PhD or MSc in clinical science

Tools

Veeva

Job description

Senior Clinical Neuro-Scientist

Gi Life Sciences Basel Vacant since : 10.11.2026 4001 Basel (BS) 100% By agreement Temporary

For Our Client, La- , 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.
• Fluency in English

Nice to Haves:

• Veeva

• Gi Life Sciences Basel
  Frau Racchi
  Consultant Life Sciences

• Work location 4001 Basel (BS)
• Workload 100%
• Employment start By agreement
• Employment duration Temporary

• By online Online form