Senior Clinical Scientist (m/f/d)

Beschreibung

As a first-tier supplier to our renowned business partner F. Hoffmann-La Roche Ltd. in Basel, we are currently looking for a motivated and dedicated Senior Clinical Scientist for a temporary assignment of 12 months.

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 Have

• Veeva

Benefits

• Work with modern and up-to-date tools in an innovative work environment
• Experience a work culture that promotes diversity and inclusion and where all employees feel valued
• Benefit from financial support for your professional development plans
• Take advantage of unbeatable, year-round discounts at renowned retailers and over 200 top brands
• Benefit from fleet discounts when purchasing new cars or receive constant fuel discounts with our fuel card
• Become part of one of the most prestigious pharmaceutical companies and actively shape the future of healthcare
• Work on a state-of-the-art campus featuring green spaces, meeting areas, and an inspiring atmosphere
• Take advantage of attractive fitness and swimming pool facilities or the gaming room as a creative retreat
• Enjoy a selection of high-quality meals in modern staff restaurants
• As part of a sustainable mobility concept, on-site parking spaces are available to you, provided you meet the relevant qualifications
• Start with a professional onboarding process and a thorough introduction to your new role during the Welcome Days

Are you interested? Don't hesitate and submit your complete application documents online today.

We look forward to hearing from you!