Senior Statistical Programmer

Company
PAREXEL
Location
Germany
Salary
Competitive
Posted
05 Nov 2018
Closes
14 Jan 2019
Ref
46430BR
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Coordinator role on projects, and liaise with sponsors, Data Operations Leads, and other functional areas as required. General areas of responsibility also include: import/export programming specification development, test data creation and test data entry, import/export programming functional testing, as well as mapping specifications to support relevant data standards.Qualifications
  • Ability to successfully work together with a global team as well as independently.
  • Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
  • Business/Operational skills that include customer focus, commitment to quality management and problem solving.
  • Good business awareness/business development skills (including financial awareness).
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Demonstrate commitment to refine quality processes.
  • Effective time management in order to meet daily metrics or team objectives.
  • Shows commitment to and performs consistently high quality work.
  • Educated to degree level in a relevant discipline and/or equivalent work experience.
  • Competent in written and oral English.
  • Excellent communication skills.
  • Relevant Clinical Trial industry experience.
  • Ability to successfully work together with a global team as well as independently.
  • Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
  • Business/Operational skills that include customer focus, commitment to quality management and problem solving.
  • Good business awareness/business development skills (including financial awareness).
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Demonstrate commitment to refine quality processes.
  • Effective time management in order to meet daily metrics or team objectives.
  • Shows commitment to and performs consistently high quality work.
  • Educated to degree level in a relevant discipline and/or equivalent work experience.
  • Competent in written and oral English.
  • Excellent communication skills.
  • Relevant Clinical Trial industry experience.

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