Clinical Scientist Neurology | Basel, Switzerland | 100%

Manpower Switzerland; Basel; Hybrid; CHF 120,000 - 170,000; Full time

Benefits offered by this job

Hybrid Working Model

Minimal travel

Job summary

Manpower Switzerland is seeking an experienced Clinical Scientist Neurology to join a global development program in Basel, Switzerland. You will contribute to Phase II/III studies, author key documents, and ensure high-quality data management and reporting.

Role requires strong neuroscience expertise, 5+ years in clinical science, and fluent English. A hybrid work model with minimal travel is offered, with January 2027 start date.

Qualifications

• Master's degree or PhD in Life Sciences, Pharmacy, Medicine, Neuroscience, or a related field.
• Minimum of 5 years as a Clinical Scientist in pharma/biotech.
• Strong experience in neurological indications including Multiple Sclerosis and/or Alzheimer’s Disease.
• Proven expertise in Phase II/III clinical development.
• Hands-on experience authoring Protocols, ICFs, CSRs.
• Excellent understanding of ICH-GCP and international guidelines.

Responsibilities

• Lead development and authoring of study documents (Protocols, ICFs, CSRs).
• Contribute scientific input to Phase II/III trial design and oversight.
• Perform clinical data review, interpretation, and reporting.
• Liaise with Data Management for data cleaning and query resolution.
• Represent Clinical Science in global Study Management Teams.
• Monitor study progress, identify risks, implement solutions.
• Present clinical findings to support decision-making.
• Provide scientific training to operations and sites as needed.

Skills

Fluent English

Communication skills

Analytical thinking

Stakeholder management

Education

Master's degree or PhD in Life Sciences/Medicine/Neuroscience

Tools

Veeva

Job description

Clinical Scientist Neurology | Basel, Switzerland | 100%

We are currently looking for an experienced Clinical Scientist to join a global clinical development program focused on neurological and neurodegenerative diseases. This role offers the opportunity to contribute to innovative Phase II and Phase III studies within a highly collaborative international research environment.

Key Responsibilities

• Lead the development and authoring of key clinical study documents, including Protocols, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), and other regulatory and operational documentation.


• Contribute scientific expertise to the design, execution, and oversight of Phase II and Phase III clinical trials.


• Perform clinical data review, analysis, interpretation, and reporting to support critical development decisions.


• Act as the primary liaison for Data Management activities, including data cleaning, query resolution, and maintaining high-quality clinical trial data.


• Participate as the Clinical Science representative within global cross-functional Study Management Teams to ensure study timelines, quality standards, and deliverables are achieved.


• Monitor study conduct and progress, identify potential risks, and implement effective solutions to ensure successful trial execution.


• Present clinical findings and support internal decision-making through clear scientific communication.


• Provide scientific training and guidance to operational teams and study sites when required.

Required Qualifications

• Master's degree or PhD in Life Sciences, Pharmacy, Medicine, Neuroscience, or a related scientific discipline.


• Minimum of 5 years of experience as a Clinical Scientist within the pharmaceutical or biotechnology industry.


• Strong experience in neurological indications, ideally including Multiple Sclerosis and/or Alzheimer’s Disease.


• Proven expertise in Phase II and Phase III clinical development.


• Hands-on experience authoring clinical study documents, including Protocols, ICFs, and CSRs.


• Strong analytical and quantitative skills with extensive experience in clinical data review, interpretation, and reporting.


• Thorough understanding of clinical development processes, study design principles, ICH-GCP requirements, and international clinical research guidelines.


• Excellent communication, presentation, and stakeholder management skills.


• Fluent English, both written and spoken.

Preferred Qualifications

• Experience with Veeva.


• Previous experience working in global multidisciplinary study teams.


• Strong problem-solving mindset with the ability to work independently and drive projects forward.

Additional Information

• Start Date: January 2027 (latest February 2027)


• Contract Duration: Until the end of 2027 with potential extension


• Hybrid Working Model: Up to 2 days remote work per week


• Travel Requirements: Minimal international travel