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Job Details

Contractor - Senior Statistical Programmer

Company: Cytel
Location:
Reference: DD CT SP
Closing Date: 01 Sep 18
Type: Contract
Salary (£): On Application
Benefits:

Job Summary:

We are seeking 4 *** Contractors *** Senior Statistical Programmers to join our FSP team based in Europe . This high visibility role 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.

Requirements:

We are seeking 4 Senior Statistical Programmers to join our FSP team based in Europe . This high visibility role 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.

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

·        Assist SDTM implementer as required

·        Create specification documents as required

·        Collaborate with NONMEM programmers as required

Your profile

• Multiple years (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 statisticians as statistical programmer in charge of a clinical trial.
• Capacity to work independently or under the guidance of a senior MSD 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.

Apply for this job: Contractor - Senior Statistical Programmer

Contact Information:

Address:  Global Headquarters
675 Massachusetts Ave. Cambridge, MA 02139 USA
MA 02139
USA
Tel:  001 617 661 2011
Fax:  001 617 661 4405
Website:  Visit Our Web Site

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