Senior Programmer - 12 Months - Pharma - Anywhere UK

Job Ref: J30878
Sector: Clinical
Sub-sector: Pharmaceuticals
Job Type: Temporary
Date Added: 08 March 2019
  • England, UK UK EC2M 4HP
  • £60 - £62 per Hour
  • Sabrina Andresen
  • 02030964701

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Senior SAS Programmer (Oncology)12 MonthsGlobal Biopharma, Full-Time (40hrs pr./week)Working home-based (UK Only)

About the Company:

We are recruiting for an experienced SAS Programmer with Late Phase experience in Oncology. We are offering a 12 months contract role of an innovative biopharmaceutical company. We are looking for someone who is strong a project level - as well as a strong communicator and collaborative person.

You would be joining a highly skilled team of programmers and statistician and would be able to influence regulatory submissions.

Your Impact:

* Collaborate with the Programming Leader to provide support for aspects of the clinical development process, including clinical development plans, regulatory submissions, commercialisation and scientific utilisation data for company products* Collaborate with the Programming Leader to provide programming support to deliver technical programming and information components of a project, including but not limited to:o Regulatory response to agency querieso Development Safety Update Reportso Periodic Benefit-Risk Evaluation Report o Investigators brochures

* Data submission strategy, i.e., legacy data, pooling data, communications with regulatory agencies* Produce and maintain the technical database standards and Programming Specification documents* Contribute to the provision of technical consulting expertise to external partners in relation to the specification and delivery of the SDTM and RDB databases by these partners* Provide support to the regulatory submissions including specification and delivery of overview databases, outputs and response to regulatory questions* Identify opportunities to improve the methodology and provide practical solutions for problems* Contribute to the development of best practice to improve quality, efficiency and effectiveness

Required Skills:

* BSc in Mathematical, Statistical, Computer Science or Life Science* Extensive SAS programming experience* Knowledge of CDSIC standard and industry best practices* Knowledgeable of the drug indications within a therapeutic area and data submission standards within that therapeutic area* Excellent communication skills* Contributes to assessing and mitigating risk within a protocol or drug project and proactively determining the need and/or level of escalation

The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.

07/04/2019 12:35:23
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