Principal Programmer 12 Months contractImmuno-InflammationGlobal Pharma, Full-TimeWork from home (UK only)Application Deadline: 21.03.2019 @5pmRequired Experience* Experience in Harp * Immuno-Inflammation experience (is desirable but not...
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.
* 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
* 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.