Dear AllStat,

 

Permanent Senior SAS Programmer position , competitive salary + excellent benefits package.

 

For a confidential consultation call Sophia Fell on:  0044 (0) 207 255 6665 or email your CV to [log in to unmask]

 

 

As a Senior SAS Programmer you will provide statistical programming support for the creation and maintenance of integrated analysis data sets for all assigned projects. This is a great opportunity for an experienced SAS Programmer to join a global biopharmaceutical company.

 

 

Accountabilities / Responsibilities:

·         Coordinate the programming activities for an individual phase I-IV clinical trial, small indication, or publication under the supervision of the Program Programmer / Group Head.

·         Lead the trial/indication team including resources planning and coordination of the different programming sites 

·         Make certain that study/indication documents and specifications are consistent and comply with company standards by providing input into Study protocol, CRF and Data structures and outputs (listings, tables and figures).

·         Program according to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-IV clinical trials and for SCS and SCE with high quality and within milestones.

·         Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.

·         Develop and comply with project/study programming standards and specifications following internal guidelines.

·         Support quality control and quality audit of deliverables. 

·         Participate as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial/indication/project level activities.

·         Track clinical trial/indication milestones for statistical reporting deliverables.

·         Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.

·         Provide input as appropriate to all meetings, discussions and activities covering all SAS programming aspects for assigned clinical trials.

·         Programming of analysis datasets, pooled datasets, listings, summaries, figures

·         Provide tables for the reporting and analysis of the clinical trials

 

Essential Skills & Capabilities:

 

·         Bachelor degree in a scientific field required, Master of Science degree preferred

·         Excellent SAS programming skills with 5 years’ experience in the pharmaceutical industry

·         Proven SAS programming experience in the area of analysing & reporting of clinical data

·         Profound knowledge in Statistics, degree in Statistics is a plus

 

 

For a confidential discussion about this or other available roles within Statistics, Biostatistics & Statistical Programming, in the first instance please contact:

 

Sophia Fell: Consultant

SEC Pharma

T: +44 (0) 207 255 6665

[log in to unmask]

www.secpharma.com

 

Best regards,

Sophia

 

 

 

 

 

 

 

 


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