Senior Statistical Programmer (m/f)

Basel  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Description


We are looking for a
Senior Statistical Programmer (m/f)

Reference: -en
Start: 03/17
Duration: 12 MM++
Place: in Basel-City
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen

Your tasks:
  • Provide high quality programming solutions and documentation to support clinical projects and the general business processes in his department
  • Interact with other members of the department and/or external business partners to clarify and assess requirements and to give advice on methodologies and tools available for data analysis, and improvement of business processes
  • Assist in the development of trial analyses and data presentations under the direction of a statistician
  • Develop and maintain specifications regarding standard data structures, software development and data transfer from external business partners to support the statistical analysis and data management (Umbrella only) of clinical studies
  • Develop software to support statistical analyses of clinical trial data
  • Analyse business processes, develop, test and validate standard software solutions to support these processes
  • Contribute to the statistical components of publications and presentations
  • Collaborate with consultants and external business partners that provide statistical and data management expertise to ensure that their contributions meet the internal standards for data structures and software development
  • Establish, promote and maintain effective working relationships with other stakeholders, departments and functions as required
  • Supervision and oversight of contractor statistical programmers


Your qualifications
  • Good knowledge regarding the development and implementation of complex data manipulation algorithms
  • Good knowledge of the principles of software design
  • Good knowledge of data modelling and relevant standard data models used to capture clinical study data
  • Good knowledge of the drug development process
  • Good knowledge of GCP and regulatory guidelines
  • Basic knowledge of statistical methods used to analyse clinical study data
  • Fluency in written and spoken English
  • Profound experience in programming SAS, other statistical software packages, and/or relational database management systems using SQL
  • Profound experience in the programming of statistical analyses of clinical study data
  • Experience as application developer, process analyst and/or application manager



Skills:
- Software developer
Start date
03/17
Duration
12 MM++
(extension possible)
From
Hays AG
Published at
01.02.2017
Contact person:
Kerstin Werner
Project ID:
1279675
Contract type
Freelance
To apply to this project you must log in.
Register