• Assistin planning and execution of programming activities for a single project.
• Assistin the review and input into project requirement including but not limitedin protocol, SAP, CRF, programming specification.
• DevelopSAS programs for SDTM, ADaM, client-defined analysis dataset, PatientProfiles, Tables, Listings and Graphs of medium-high complexity within asingle project in support of Statistical Analysis Plan, posters,Integrated of Summary of Safety(ISS) and Integrated Summary ofEfficacy(ISE).
• Supportdata management by generating data listings. Interact with Biostatisticsand Regulatory to design and prepare regulatory submission-ready packages.
• Actas a Lead programmer for low-medium complex projects.
• Developproficiency in mock up shell development.
• RepresentStatistical Programming at internal and client meetings.
• Actas a Statistical Programming consultant to clients and internal customersin related disciplines e.g. Clinical Data Management, Project Management.
• Ensurequality of personal work and the work of the team when acting as a LeadProgrammer.
• Prioritizepersonal workload and that of teammates; Perform work with minimalsupervision.
• Workon complex problems where analysis of situations or data requires anevaluation of intangible variables; development of technical solutions toabstract problems which require the use of ingenuity and creativity.
• AdviseSenior Statistical Programming Staff of changes in scope of projects toenable the timely development of change orders.
• Goodexperience with CDISC standards including Define.xml files.
• Reviewdraft and final production runs for low-medium complex project to ensurequality and consistency.
• Carryout all activities according to R&G SOPs working within the frameworkof the Quality management System and to Good Clinical Practice (GCP).
• Demonstratefull proficiency in technical/programming skills.
• Contributebroad knowledge of clinical trial activities.

Other Accountabilities & Tasks

· Assist with interviewing and selection of potential candidates

· Provide ongoing training and mentoring within Statistical Programming toensure thorough knowledge of the processes used and ongoing technicaldevelopment.

· Perform other duties as requested by management.

MINIMUM REQUIREMENTS

• Bachelor’sdegree and/or equivalent in computer science, statistics, mathematicsor other scientific field (or equivalent theoretical/technical depth). Master degree is preferred.
• At least 3 year SAS programming experience, preferably in a pharmaceutical/clinical trialenvironment.
• Fluentin written and spoken English
• Demonstrateadvance SAS skills good macro programming and SAS/STAT.
• Independentlyand fully to lead middle complex project