Senior Statistical Programmer – Switzerland

Mylene Paumier at CK Clinical is recruiting for a Senior Statistical Programmer to join a global pharmaceutical company at their site, based in Switzerland, on a permanent basis.

Responsibilities

As Senior Statistical Programmer, your responsibilities will include:

  • Coordinate the programming activities for an individual phase I-IV clinical trial, small indication, or publication under the supervision of the Program Programmer / Group Head.
  • Lead the trial/indication team including resources planning
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    and coordination of the different programming sites
  • Make certain that study/indication documents and specifications are consistent and comply with company standards by providing input into Study protocol, CRF and Data structures and outputs (listings, tables and figures).
  • Program according to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-IV clinical trials.
  • Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.
  • Develop and comply with project/study programming standards and specifications following internal guidelines.
  • Support quality control and quality audit of deliverables.
  • Participate as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial/indication/project level activities.
  • Track clinical trial/indication milestones for statistical reporting deliverables.
  • Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
  • Mentor junior programmers.

Qualifications

As Senior Statistical Programmer, you will have the following qualifications, skills and experience:

  • University/Bachelor/Master’s degree in Mathematics, Statistics, Data Analysis Program or Computer Science (or equivalent degree with experience).
  • Fluent English (oral and written)
  • Ability to coordinate programming work across a clinical study.
  • Experience using SAS in the analysis and the reporting of pharmaceutical data (in Oncology therapeutic area would be desirable)
  • Working knowledge and expertise with SAS (including SAS macro language)
  • Working knowledge of database design/structures
  • Good understanding of global clinical trial practices, procedures and methodologies.
  • Good understanding of regulatory requirements (e.g. GCP, ICH)Mylene Paumier at CK Clinical is recruiting for a Senior Statisticial Programmer in Switzerland

How to apply

For more information or to apply for this Senior Statistical Programmer position, please contact Mylene Paumier on +44 (0)207 470 5672 or email: mpaumier@ckclinical.co.uk. Please quote reference CL25700 in all correspondence.

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