Contract Senior Statistical Programmer

Location
Switzerland
Salary
Competitive
Posted
17 Dec 2018
Closes
13 Feb 2019
Ref
WOB61
Contract Type
Contract

Contract Senior Statistical Programmer

Our client is looking for a contract Senior Statistical Programmer for an initial 12 month contract, with the possibility of another years extension, to be office based in Switzerland for a large pharmaceutical company. The role requires someone with strong technical programming skills and professional knowledge, a proven ability to deliver results, strong customer focus alongside excellent planning and organisational skills.

Key Responsibilities:

  • Reviews clinical protocols with respect to statistical programming deliverables.
  • Reviews and provides input into the Statistical Analysis Plan (SAP) and based on the SAP, provides input into the programming plan for a study or project.
  • Reviews and provides input into Case Report Froms (CRFs) and external data transfer specifications.
  • Reviews SDTM specifications and provides comments on SDTM datasets when issues / inconsistencies are identified.
  • Develops, verifies and maintains analysis dataset specifications and metadata according to the required internal and external standards (ADaM).
  • Designs and develops statistical programs in support of clinical research, safety and efficacy analysis and reporting activities.
  • Performs quality control in support of clinical research analysis and reporting activities.
  • Maintains documentation as appropriate.
  • Completes programming tasks of medium to high complexity with high quality and timeliness of deliverables.
  • Critically reviews requirements and data, identifies gaps, suggests solutions, and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
  • Prepares analysis dataset electronic submission deliverables according to industry requirements (ensures necessary compliance checks are performed and issues addressed).
  • Represents the statistical programming study team at trial team meetings and discusses data presentation and analysis methods with the appropriate members of the programming and clinical trial team.
  • Informs and suggests solutions to the programming project or therapeutic area lead on critical programming issues within the project.
  • Provides technical advice and support to other team members.
  • Assesses, recommends and contributes to the development of new standards, policies and procedures.

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