Senior Clinical Scientist

Main Responsibilities:

• 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.
• 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.
• Be the main point of contact for data management regarding periodic clinical data review and data cleaning
• 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)
• Provide training and science input to operation colleagues and study site staff, as agreed with clinical operations
• 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.
• Bring a positive, energetic, responsible, creative, curious and solution-seeking mindset and proactively contribute to interdisciplinary clinical project teams with integrity, passion and courage.

Qualifications and Experience:

• 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, while experience with Veeva is a nice to have