Dear Allstat,

Our client is looking for a Statistical Programmer to join their UK based programming team 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 represent the Programming and Technical Support team on international teams and working groups.

Duration: 12 month contract
Location: South East UK
Rate: £45-52 per hour

Responsibilities:

- Responsible for technical design, programming and QC of SAS programs for the management, reporting, analysis and submission clinical trial data.  Accountable for ensuring compliance with ICH GCP, relevant SOPs and guidelines and standards.
- Where assigned the Programmer role for the study, take on the global responsibility for the programming tasks, including planning, the provision of programs to assist in ensuring data quality and reporting of the data. Be fully responsible for the quality of the analysis data.  Be fully responsible for the quality of the analysis data, data displays and derived submission data.
- To use SAS to meet the business needs of Biometrics and Data Management.
- Ensure agreed timelines relating to reporting of data are archived in accordance with Corporate Guidelines for Clinical Development.
- Plan resources required to meet timelines for clinical trials assigned to as the programmer
- Liaise with the Data Manager and Statistician as required to ensure programming is effective in the support of data quality, reporting and analysis across the trial.
- Collaborate with departments internationally and the trial team to facilitate the achievement of agreed objectives.

Background required:

- Comprehensive understanding of the Biometrics and Data Management aspects of ICH GCP Guidelines for clinical development, using SAS to manage, report and analyse clinical trials data, good programming practice and QC/validation requirements.
- The use of SAS in a clinical trials environment.
- Understanding of and ability to assume QC and validation responsibilities in line with department objectives.
- Proven interpersonal, communication, presentation and coordination skills required to be an effective member of the trial team, in the UK and internationally if selected.

Invitations are invited from EU nationalities only as sponsorship cannot be given for this position.

If you are interested in this vacancy then please contact Tim Barratt at Key People on: 

[log in to unmask]  or by telephone on +44(0)1727 817 626

You can see our other vacancies at www.keypeople.co.uk 

Kind regards
Tim Barratt
Recruitment Resourcer
Key People Ltd
Catherine House, Adelaide St, St Albans, Herts, AL3 5BA
Direct Tel: 01727 817 626 / Office: 01727 811634 / Fax: 01727 844838
E-Mail: [log in to unmask] / Web Page: http://www.keypeople.co.uk/
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