Afternoon All

 

Please see below details of a UK based vacancy, with the option to work from home.

 

Senior SAS Programmer – UK office with flexibility

UK

 

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

 

Summary:

SEC Pharma is currently recruiting for a Senior SAS Programmer to work for a leading clinical trials organisation in the UK (M4 Corridor). Flexibility is possible in this role, 2 to 3 days working from home will be considered for the right candidate.

 

Requirements:

As Senior Programmer you will provide programming and technical support to allocated studies within agreed project timelines. Communicate programming related study issues to the Study Statistician, participate in business development and client liaison as required.  You will contribute towards technical leadership within the SAS programming team and ensure that clinical trial outputs included in the study report are reliable and accurate. You will also act as point of contact for both internal and external customers for all statistical programming issues for allocated studies.

Your duties include;

 .   Produce and QCs datasets, tables, figures and listings using SAS, including routine statistical analyses.

 Programmes electronic data checks as required.

 Liaises with external suppliers for receipt of electronic data as required.

 Performs ad hoc programming tasks to assist the Head of Statistics with data review.

 Reviews statistical content of the CSR.

 Liaises with Data Management to ensure accurate derivation of statistical output from CRF data.

 Adheres to scope of work, budget and timelines for all study related activities and flags potential changes in scope.

 Proactively communicates database and programming issues to internal and external study teams and suggests resolutions.

 Represents the statistics team at sponsor meetings as required.

 Attends study team meetings throughout the life of the study to proactively communicate issues that may affect the data management of the study.

 Provides solutions to issues that arise during the conduct and analysis of the study.

 Manages the flow of work for allocated studies, adheres to agreed project timelines and flags potential problems.

 Reviews and update SOPs.

 Leads process improvement initiatives in area of expertise.

 Maintains up to date knowledge of relevant regulatory guidance and requirements.

 Provides in-house training, technical support and mentoring for colleagues.

 Provides business development support and attends bid defence meetings as required.

Qualifications:

. Graduate, postgraduate, 4-year college degree, or equivalent, in a relevant scientific discipline.

 Relevant programming experience within the pharmaceutical industry or clinical research organisation.

 Experience in the production and QC of datasets, tables, figures and listings to summarise and analyse clinical data using SAS.

 Professionally autonomous across diverse and complex programming projects

 Knowledge of the clinical development process and its critical paths.

 Knowledge of ICH GCP.

 Experience of working in multi-disciplinary teams.

 

 

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