Clinical Biostatistician 80 - 100

Our Client

Our client is a leading Clinical Research Organization (CRO) dedicated to improving global health by providing highquality clinical research services. The team of experts collaborates with pharmaceutical biotechnology and medical device companies to design manage and analyze clinical trials ensuring that new therapies reach the patients who need them most. Location: Basel / hybrid

Tasks

• Design and develop statistical analysis plans for clinical trials including sample size calculation randomization and interim analysis
• Perform statistical analysis and interpretation of clinical trial data ensuring compliance with regulatory requirements and guidelines
• Collaborate with clinical and project teams to provide statistical input on study design protocol development and data management
• Prepare and review statistical sections of clinical study reports publications and regulatory submissions
• Ensure the quality and accuracy of data through robust statistical methods and best practices
• Assist in the development of standard operating procedures (SOPs) related to biostatistical analysis
• Stay uptodate with the latest developments in biostatistics and clinical research to ensure the application of innovative methodologies

Requirements

• Masters or Ph.D. in Biostatistics Statistics Mathematics or a related field
• Minimum of 35 years of experience as a biostatistician in a clinical research setting preferably within a CRO or pharmaceutical company
• Proficiency in statistical programming languages such as SAS R or Python
• Strong understanding of clinical trial design analysis and regulatory guidelines (e.g. ICH FDA EMA)
• Excellent analytical and problemsolving skills with attention to detail
• Strong written and verbal communication skills with the ability to explain complex statistical concepts to nonstatisticians
• Ability to work independently and collaboratively in a fastpaced environment
• Experience with CDISC standards (SDTM ADaM) is a plu

Benefits

• Opportunity to work on cuttingedge clinical trials and make a real impact on patient outcomes
• Collaborative and supportive work environment that values innovation and professional growth
• Competitive salary and benefits package including health insurance retirement plans and paid time off
• Flexible work arrangements including remote work options.
• Commitment to diversity equity and inclusion in the workplace

If you are interested in this exciting challenge please apply online to Mr Kelaja Wick. You can also find other exciting vacancies and more information about the application process on our website. We look forward to meeting you in person soon. Discretion is our capital.