Description
Senior Statistical Programmer Analyst (m/f)
Reference: -en
Start: 09/18
Duration: 12 MM++
Main tasks:
- Responsible for statistical programming support for the Pharma Development organization
- Provide end to end statistical programming support in planning, specifying, designing, developing and implementing statistical software solutions for the reporting and analysis of clinical trials in accordance with applicable processes
- Capable of leading statistical programming activities at study level or part of clinical project and prepares summarized information for clinical study team members
- Assess and clarify requirements, develop programming specifications and statistical programming solutions to meet the project requirements
- Provide proactively and independently technical solutions to a wide range of problems
- Build and maintain effective working relationships within cross-functional teams
- Adapt to changing circumstances, policies, work assignments & team members
- Explore new ways of working based on changing of these business needs
Main qualifications
- BA, BS or advanced degree in mathematics, statistics, biological sciences, computer science or equivalent experience
- Profound SAS programming experience in clinical research preferably with emphasis in the development and support of the analysis of clinical trial data
- Optional: Experience of R programming and of proactive data visualization to support experts in other fields in their decision making
- In depth experience in reporting clinical studies and pooling clinical data
- Knowledge of statistical concepts (p-values, rates and proportion, frequencies, confidence intervals, survival analysis, non-parametric analysis)
- Capable of implementing these ideas in clear, efficient SAS or R programs
- Expertise in relevant operating systems (Windows/UNIX) and in depth knowledge of Pharma industry data standards, such as CDISC/SDTM & ADaM and FDA/ICH guidelines
- Proficient in problem solving and able to efficiently debug and resolve issues in programming code produced by others
- Ability to meet timelines when working on multiple tasks simultaneously and experience on how to effectively prioritize tasks and project manage to optimize support
Main advantages:
- You will work in an international environment
- Pleasant working atmosphere
- Good infrastructure
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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My contact person:
Selina Denise Schweizer
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