The RWE Programming roles will provide statistical programming expertise, informing data harmonization for primary data and secondary data from multiple sources (EMRs, PROs, eCRF, Observational studies, etc.
advise on database design and data collection, and the programming of tables, listings and figures using SAS (Base SAS, SAS / STAT and SAS Macro) and other applications.
These are exciting new solution-driven roles within the team as RWES expands into developing further innovations for clients.
RESPONSIBILITIES FOR LEVEL I & II :
Develops, executes and reviews programs to provide statistical programming support for statisticians, clients, or business demands to source, organize (creating statistical tables, listings, and graphs) and interpret complex data sets.
Conducts statistical analyses for client reports and publications and utilize findings, and insights for practical application to further business operations, come across innovative findings and discoveries for solution and product development
Perform the programming quality control checks for the source data and report data issues periodically
Detect errors in detail and correct. e.g., review tables / listings, edit checks output and SAS programs to ensure quality of deliverables
Assist in the development of programming documentation including specifications, as appropriate, under supervision
Provide advanced technical expertise in conjunction with internal and external clients, and bring project solutions to teams and department, under supervision
Develop, implement and validate new process technologies, macros and applications under supervision
Fulfil project responsibilities at the level of assisting the statistical programming team lead
Understand timelines for and milestones affecting their work and alert supervisor to potential slippage
ADDITIONAL RESPONSIBILITIES FOR LEVEL II :
Responsibilities for level II roles are similar to level I but will require additional planning activity, independent working, reporting to internal and external clients and, from time to time, acting as technical lead.
MINIMUM SKILLS, EXPERIENCE & QUALIFICATIONS FOR STAT PROG I & II :
Knowledge of statistics, programming and / or clinical drug development process
Working knowledge of computing applications such as Base SAS, SAS / STAT and SAS Macro Language
Working knowledge of the SDTM structure
Working knowledge of the ADaM standards
Basic knowledge of applicable clinical research regulatory requirements would be an advantage; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Excellent accuracy and attention to detail
Good organizational, interpersonal, leadership and communication skills
Ability to effectively handle multiple tasks and projects, under supervision if required
Ability to establish and maintain effective working relationships with co-workers, managers and clients
Master's Degree Computer science or related field and 1 years relevant experience Or Bachelor's Degree Computer science or related field and 2 years relevant experience Or Equivalent combination of education, training and experience
ADDITIONAL SKILLS, EXPERIENCE & QUALIFICATIONS FOR STAT PROG II :
In-depth knowledge of applicable clinical research regulatory requirements would be an advantage; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to implement programming specifications as appropriate
Ability to estimate programming scope of work and assist in communicating project status
Able to solve complex problems
Ability to recognise when negotiating skills are needed and seek assistance when required
Additional 1 years work experience for those holding a Bachelor’s Degree, so 3 instead of 2.
WE OFFER :
Competitive salary and benefits package
The opportunity to be part of a friendly and supportive team
Opportunity to work on complex trials in challenging therapeutic areas