Dear Allstat,

CK Clinical is recruiting for a Statistical Programmer to work on contract for a leading Pharmaceutical organisation in the UK on an initial 6 months basis. The purpose of the role is to coordinate the programming aspects of assigned clinical trials and to develop programs and tools for the management, reporting and analysis of clinical trial data. Additionally, you will also represent the Programming and Technical Support team on international teams and working groups.

Main responsibilities includes:

* To be responsible for the technical design, programming and QC of SAS programs for the management, reporting, analysis and submission clinical trial data. Be accountable for ensuring compliance with ICH GCP, relevant SOPs and guidelines and standards.
* Be fully responsible for the quality of the analysis data, data displays and derived submission data.
* Ensure agreed timelines relating to reporting of data are achieved in accordance with Corporate Guideline for Clinical Development.
* Review and contribute ideas to processes.
*Plan resources required to meet timelines for clinical trials.
* Plan and conduct training sessions in accordance with new SAS versions, new SAS utilities and to new hires and less experienced programmers
* Ensure specifications provided and developed support the efficient programming of the reporting and analysis of the data and development of standardised submission data
* Develop and optimise communication with the trial team and local management, to ensure that all functions are aware of trial related topics such as data import into the SAS environment, programming for data quality review, reporting, analysis and submission of data so that they are delivered in terms of time and quality
* Participate in trial planning meetings as required
* Liaise with Data Management & Statistics as required to ensure programming is effective in the support of data quality, reporting and analysis across the trial.

Interested applicants should be a graduate in a Statistical, Mathematical, Computing / Information Science or Life Sciences subject (OR Equivalent). You will have proven experience of working within the Pharmaceutical industry as a Statistical Programmer and have proven experience of using SAS. You will also have Knowledge and experience of clinical trial conduct and methodology, ICH-GCP and EU Directives. Applicants should also hold proven interpersonal, communication, presentation and coordination skills and have the ability to present specialist/technical information to audiences involved with clinical trials.

Rates on offer are excellent and can be discussed upon application.

For a confidential discussion or further information, please call +44(0)1438 870028 or email an updated copy of your CV to [log in to unmask]<mailto:[log in to unmask]>

Best wishes,

Priya

Priya Mukherjee BSc (Hons) MIRP CertRP
Senior Consultant

CK Clinical Limited
9 High Street
Stevenage Old Town
Hertfordshire
SG1 3BG

DD: +44 (0)1438 870028
Mobile: +44 (0) 7714 288632
Tel: +44 (0)1438 743047
Fax:+44 (0)1438 723800



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