Dear Allstat,
CK Clinical are recruiting for a Senior Technical Programmer to work for a leading Pharmaceutical organisation in the South-East, UK. The purpose of the role is to provide statistical software and software documentation support to specific clinical projects. You will take responsibility for the planning, development, validation, documentation and maintenance of generic tools across project programs, and ensure that objectives, standards, deadlines and other requirements set are attained. You will also advise on SAS software usage and problem solving.
Key Responsibilities:
* Provide technical advice and support of members within biometrics.
* Assess, recommend and develop new standards, policies and procedures.
* Keep abreast of statistical programming methodology, applications and software developments.
* Maintain familiarity with regulatory authority guidelines relating to biometrics, data reporting and medical issues in project areas.
* Maintains proficiency with respect to in-house computer facilities and software.
* Participates in and contributes to internal training programs.
* Makes presentations at professional forums.
* Develop and document statistical programming standards in accordance with current statistical programming practices and regulatory authority requirements.
* Program, validate and document software in SAS following statistical programming standards and ensures its availability to users.
* Train users to apply statistical programming standards and standard software.
* Assist users to resolve individual technical difficulties with the standard software.
* Programs, validates and documents data tabulations, graphics and statistical evaluations for efficacy and safety. Ensure that programs developed for specific projects are sufficiently portable to allow application to other projects and protocols.
* Perform analyses of efficacy and safety data, generates tabulations and graphs and provides them to member of the biometrics team.
* Provide SAS datasets in formats required for special evaluations.
Interested applicants should be qualified to degree level in IT, Life Science, Statistics, Computer Science, Mathematics (or other related discipline). You will have proven previous experience of working as a Programmer ideally within clinical research and drug development. You will be confident in the use of computers and can readily learn new software applications. You should have experience in programming and using statistical software as well as good knowledge of databases and interface systems. Strong SAS knowledge is recommended.
You will also hold excellent communications skills and should be able to establish and maintain good working relationships.
For a confidential discussion or further information, please contact Priya Mukherjee on +44(0)1438 870028 or email an updated copy of your CV to [log in to unmask]<mailto:[log in to unmask]>
Have a good weekend,
Best regards,
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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