Statistical programmers for late stage clinical trials

Région
Woluwe (Brussels)
Publication
mercredi 9 mai 2018
Date limite
samedi 9 juin 2018
Réf
7F452XPE-BE
Contact
Andrea Baetens
Fonction
Autre
Niveau d'expérience
2 à 5 ans d'expérience
Type de contrat
CDI
Temps de travail
Temps plein
eXPErt services for eXPErt professionals.
That's XPE. For one of our clients we are looking for: Statistical programmers for late stage clinical trials Organisation description:

XPE Pharma & Science is looking for Statistical Programmers, for one of our clients, a pharma company located in Woluwe.


The services on this assignment will be in support of existing project teams, planning, interpreting and the results on late stage clinical trials for use in Health Technology Assessment Dossiers (addressing HTA specific clinical objectives). The searched services will be in statistical programming using SAS on randomized clinical trials.

Job description:

This project will take 6 to 8 months. Were you can work from home 2 days a week.

4Main responsibilities for this mission consists in updating existing ADaM analysis datasets (based on requirement from statistics) and identified key analysis programs (with creation of Tables, Figures, Listings and a related user guide) as well as developing new project specific AdaM analysis datasets and analysis programs. Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have. SAS/MACRO is a must for this mission. Capacity to interface with statisticians as statistical programmer in charge of a clinical trial. Team oriented person. Capacity to work independently or under the guidance of a senior statistical programmer. Capacity to quickly read SAS code (including MACRO code) developed by others and understand them in the context of clinical trials. Knowledge and practice of CDISC SDTM and ADaM data standards. ADaM is a must have for this mission. Ability to work complying to the company programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs. Strong and proven experience of work with late stage clinical trial data in support of safety and efficacy analysis. Oncology therapeutic area experience is an asset. Fast learner, team oriented, able to work independently. Able to read, write and speak fluently in English. English writing skills are a must for this mission.

Profile:

• Multiple years (preferably min 5) of relevant late stage clinical trial SAS statistical programming experience in analysis and reporting.

• Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a plus. SAS/MACRO is a must for this mission.

• Capacity to interface with clinicians and statisticians as statistical programmer in charge of a clinical trial.

• Capacity to work independently or under the guidance of a senior statistical programmer.

• Capacity to quickly read SAS code (including MACRO code) developed by others, understand them in the context of clinical trials and adjust to address the business question.

• Knowledge and practice of CDISC SDTM and ADaM data standards. ADaM is a must have for this mission.

• Ability to work complying to the company programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs.

• Strong and proven experience of work with clinical trial data in support of safety and efficacy analysis.

• Analyst: Able to contribute to the finalization of Programming Requirement Specifications based on study documents and minimal guidance from the programming and statistics project leads.

• Fast learner, team oriented, able to work independently.

• Able to read, write and speak fluently in English. English writing skills are a must for this mission.

• Experience with SAS on PC and UNIX platforms


Offer:

Launch your career as a Statistical Programmer at XPE Pharma & Science and become our XPErt consultant in statistics for pharmaceutical companies. During your project our Talent Manager will guide you and work together for your career path. For this position we have a very interesting salary package with loads of extra-legal advantages (company car, mealvouchers, eco vouchers,...) .




Licenses
XPE Personnel Services NV/SA: Flanders: VG15/BU, Brussels: B-AA5.031, Wallonia: W.RS.002/W.INT.002
XPE Group NV/SA : Flanders: VG1834/B, Brussels: B-AA11.007, Wallonia: W.RS.713

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