Senior Project Manager Medical Statistics
Dübendorf, CH
In this role you will be required to
Statistical Analysis of Clinical Data:
• Develop statistical analysis plans (SAPs) and execute statistical analyses in a correct and timely manner
• Methodological and statistical support for clinical studies according to project milestone plan
• Sample size calculation and input to and review of study protocols for projects in the planning phase
• Develop monitoring statistics, sample size re-estimation and interim-analyses as appropriate for projects in the monitoring phase
• Develop final analyses, final statistical reports as well as support publications for projects in the analysis phase
Statistical Support for AO ITC:
• Statistical consultancy for Project Managers and Principal investigators
• Make complex statistical analyses comprehensible to laymen and translate their results into recommendations for clinical practice
• Facilitate publication of scientific results within AO ITC (peer-reviewed publications, presentation at international meetings)
• Statistical analysis of non-clinical data
Back up/Support of Statistical Programmer:
• Ensure high quality standards for statistical programming and data management/monitoring activities
• Create, validate and manage statistical codes for study-related activities, incl. monitoring activities (e.g. reports, grahps, listings)
• Implement codes according to data management plans (DMPs) and statistical analysis plans (SAPs)
• Develop, program and validate data validation plans (DVPs)
Collaboration with External Partners:
• Statistical consultancy for external partners, including support for peer-reviewed publications
Quality Management:
• Assist in optimizing quality standards and SOPs related to medical statistics
In General:
• Functional lead of the statistical team, including resource planning and lead in the stats team meetings
• Support Head Medical Affairs in strategical decisions related to statistical team (e.g. development of statistical budgets)
• Develop and maintain standard operating procedures (SOPs) related to statistics
• Statistical consultancy for external partners, including support for peer-reviewed publications
To master this challenge you have
Education:
• MSc degree in statistics or equivalent qualification (eg. GradStat) combined with a minor degree in a biomedical discipline
Job specification:
• Sound SAS or Stata programming skills
• Leadership experience with at least 3 years experience in analysis of clinical research data
• Good knowledge of statistics
• Numerical and analytical skills
• Attention to detail and reliability
• Flexibility and customer-focused mindset
• Ability to work both independently and in a team
• Good writing skills scientific publications
• Strong oral communication skills in German and English
We offer
- An interesting and varied job in an exciting and innovative organization
- The opportunity to be part of a highly committed international team
- Modern infrastructure
- Employment conditions which match the requirements and offer a high degree of flexibility regarding working hours and location