Project Manager Medical Statistics
Employment Type:
Permanent
Part-time percentage:
100%
This position is located in:
Zizers, CH
Experience level:
Experienced professional
Please send us your application documents in:
English
In this role you are required to:
Correct and timely execution of all kind of statistical input as needed for clinical research activities within and for AO ITC, such as
- Medical statistical input and review as needed for One-pagers, Research Summaries and Study Protocols for clinical research projects conducted by AO ITC Clinical Evidence
- Develop statistical analysis plans, monitoring statistics, sample size re-estimation, interim analyses as appropriate for clinical research projects conducted by AO ITC Clinical Evidence
- Development of codes / programming for statistical analysis according to SAPs as well as development of TLFs
- Validation of programmed analyses as applicable
- Final analyses, final statistical reports input and review and support for publications for clinical research projects conducted by AO ITC Clinical Evidence
- Review of data bases and DVPs
- Additional statistical activities
- Statistical consultancy for Project Managers and principal investigators
- Make complex statistical analyses comprehensible to laymen and translate their results into recommendations for clinical practice
- Statistical analysis of non-clinical data, such as surveys
- Statistical analyses needed for validation of fracture classifications or score validation
- Supporting the development and maintenance of standard operating procedures (SOPs) related to statistical activities in AO ITC Clinical Evidence and according to the needs guided by the Quality Manager AO ITC Clinical Evidence
To master this challenge you have:
Education and Job Specification:
Education:
MSc degree in statistics or equivalent qualification (eg. GradStat) combined with a minor degree in a biomedical discipline
Job specification:
- Advanced SAS programming skills; Stata programming skills beneficial, but not mandatory
- At least 3 years experience with 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
Date of publication:
Jun 23, 2022