Location: Paris, Fr / Geneva, Sw / Barcelona, Sp
Closing Date: 23 Dec 16
Type: Full Time
Salary (£): Competitive
BA?BSc or higher qualification Office based in Europe Barcelona, Paris or Geneva Experience within Clinical development CDISC Team lead
Senior Statistical Programmer
We are seeking a Senior Statistical Programmer to join our team based here in Europe in either Paris, Barcelona or Switzerland. This high visibility role is responsible for data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, including, but not limited to creation of analysis files, tables, listings, and figures, validation of those files, maintenance of associated tracking and validation documentation, and the creation and validation of CDISC, SDTMs and ADaM.
You will provide technical and process-related guidance to team members and be tasked with leading lead sub-team projects with minimal or no supervision. A majority of your work will be hands-on statistical programming, and you will be expected to perform complicated programming tasks quickly and efficiently. You should feel comfortable working in a team environment, where team members may be distributed globally.
Additional responsibilities include:
Lead small team projects
Assist in some of the tasks of the Study Lead Programmer when requested
Provide guidance to Study Programmers when requested
Interact and collaborate with study team members from other functions
Create specification documents as required
Experience within Phase I-III
The position can be home based (for experienced candidates) or in one of our offices within Europe.
Qualifications and Experience
You will have a BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject, relevant career within statistical programming experience in a clinical development environment. Additionally, we require:
Excellent SAS data manipulation, analysis and reporting skills
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Excellent oral and written English communication skills
Ability to provide quality output and deliverables, in adherence with challenging timelines
Willingness and ability to learn and follow Company’s standard processes and procedures.
Ability to lead small team projects effectively
Ability to effectively perform complex statistical programming and related tasks
Willingness and ability to provide guidance to team members on technical and process questions
Strong ability to implement the latest CDISC SDTM, CDISC ADaM, and Define standards
Compensation & Benefits
We offer a competitive salary-based package, along with bonus, comprehensive medical/healthcare insurance, plus a contributing pension.
ICC, Bat. C, 2nd floor, Route de Pré-Bois, 20 C.P. 1839, 1215 Geneva 15, Switzerland
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