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Contract Statistical Programmer - Geneva/Paris/Barcelona in Genève, Switzerland

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Location
Genève, Switzerland
Salary
Negotiable
Job type
Contract, Temporary
Category
Engineering/Development, Clinical/Medical
Job Id
170417-5
Posted on
18 Apr 2017
View all Jobs from CK Group

About the Role:

Laura Christie is currently recruiting for contract Statistical Programmers for one of the leading Biometrics CRO's in the world. The locations of these role will be in Switzerland, France, Spain or potentially home based.

Main duties and responsibilities:

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.

Leading small team projects.

Assisting in some of the tasks of the Study Lead Programmer when requested.

Providing guidance to Study Programmers when requested.

Interacting and collaborating with study team members from other functions.

Creating specification documents as required.

Experience within Phase I-IV.

Key requirements:

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.

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.

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.

Excellent oral and written English communication skills.

A full job spec is available upon request

For more information or to apply for this role, please contact Laura Christie on [... Click Apply...]928 or email [... Click Apply...]. Alternatively, please click on the link below to apply online.

CK Clinical is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL37560 in all correspondence.

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