Dear Allstat,

 

CK Clinical is currently recruiting for a SAS Programmer to work for a leading pharmaceutical organisation in the UK. You will provide statistical software and software documentation support to the programming group in general and to specific clinical projects. You will also ensure that the objectives, standards, deadlines and other requirements set by management with respect to statistical software and software documentation are attained.

 

Principle responsibilities:

 

· Provides advice and support to members of biometrics.

· Assesses, recommends and develops new standards and policies.

· Assesses, develops and documents new methods and software.

· Keeps abreast of statistical programming methodology, applications and software developments through literature and attendance at meetings.

· Maintains familiarity with regulatory authority guidelines relating to biostatistics, data reporting and medical issues in project areas.

· Develops and maintains proficiency with respect to in-house computer facilities and software.

· Interacts with members of biometrics to ensure good coordination and communication.

· Participates in and contributes to internal training programs.

· Develops and documents statistical programming standards in accordance with current statistical programming practices and regulatory authority requirements.

· Programs, validates and documents software in SAS following statistical programming standards and ensures its availability to users. Whenever creating new software, ensures the efficient use of existing software.

· Suggest new tools/enhancements to existing tools, and/or able to work on tool development

· Ensures that activities performed within the project are executed in a timely manner and to the required high statistical and reporting standards.

· Interacts with other members of biometrics and with the study team to clarify and assess programming requirements.

· Assists in the development of trial analyses and data presentations relating to efficacy and safety data under the direction of a senior programmer

· Creates the dataset specifications according to the applicable data model in cooperation with clinical programming.

· Provides SAS datasets in the format required for special evaluations.

· Programs, validates and documents data tabulations, graphics and statistical evaluations for efficacy and safety.

. Ensures that programs developed for specific projects/protocols are sufficiently portable to allow application to other projects and protocols.

 

Interested applicants will be qualified to Degree level in IT, Life Sciences, Statistics, Computer Science, Mathematics or other analytical field (OR Equivalent). You will have proven experience of working as a SAS Programmer within a Pharmaceutical/CRO/Biotechnology organisation together with strong knowledge/experience of international clinical research and drug development. You will be confident in the use of Computers; can readily learn new software applications, and hold proven experience in the use of statistical software as well as knowledge of databases and interface systems.

 

For immediate consideration, please send an updated CV to [log in to unmask] or call +44(0)207 470 5673 for a further discussion.

 

I look forward to hearing back from you.

 

Kind regards,

Priya

 

Priya Mukherjee BSc (Hons) MIRP CertRP

European Operations Manager

 

CK Clinical Limited

Crown House

72, Hammersmith Road

London

W14 8TH

 

DD: +44 (0)207 470 5673

Mobile: +44 (0)7436 104 960

Tel: +44 (0)207 470 5670

Fax:+44 (0)207 470 5671