Description
Hays ist ein weltweit führender Personaldienstleister, der sich auf die Rekrutierung von Spezialisten konzentriert - sowohl für den Projekteinsatz als auch für Festanstellungen und auf Zeit. In Deutschland, Österreich und der Schweiz vertrauen mehr als 600 internationale Topunternehmen auf unsere qualitätsgesicherten Prozesse, wenn Sie Experten suchen.We are looking for a
Senior Statistical Programmer Analyst - Early Development (m/f)
Referenz: -en
Beginn: 07/12
Dauer: 24 MM+
Ort: in Switzerland
Branche: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Lead statistical programming activities on a set of clinical studies
- For clinical study data ensure the data is appropriately collected and the data sets provided by clinical programming are acceptable for the intended analyses
- Prepare data derivations and summaries, including graphics and provide information to clinical study team members
- Responsible for accuracy and reliability of results
- Build and monitor quality in every aspect of job activities, and by adhering to the risk based quality control processes
- Ensure adherence to statistical programming standards, effective use of available standard programs and compliance with Standard Operating Procedures and internal guidance documents
- Build and maintain effective working relationships within the cross-functional teams
- Develop timelines for SPA component of the studies and negotiate effectively with study teams for reasonable timelines and scope, also negotiates alternative timelines based on resourcing / priority constraints
Ihre Qualifikation
- Advanced knowledge of SAS programming techniques, such as complex SAS macros, advanced SAS/GRAPH; knowledge of SAS statistical procedures
- Knowledge of statistical concepts, such as p-values, rates and proportion, frequencies, confidence intervals, survival analysis, non-parametric analysis
- Capable of implementing these ideas in clear, efficient SAS codes for the purpose of data analysis and reporting
- Familiar with relevant operating systems (e.g. UNIX)
- Has a good understanding of data collection and database concepts including data flows in clinical trials
- Had exposure to Pharma industry data standards, such as CDISC SDTM and ADaM data models
- Knowledge of FDA/ICH guidelines
- Experience in supporting regulatory submissions and regulatory deliverables (e.g. health authority questions)
- Experience in handling biological data of various kinds (e.g. PK/PD data, genomic/genetic/protein biomarker data)
- Able to communicate clearly and without ambiguity using fluent spoken and written English
Skills:
- Biostatistician
Keywords: Clinical data analyst SAS specialist Clinical data specialist freelance contractor freelancer contract contr contracting self-employed project Projekt