Computer Programmer |Senior|

Our Client from an Apparel & Fashion company is looking for a Senior Computer Programmer. You are responsible for all aspects related to programming activities for the data preparation and analysis of clinical data. Duties include creating all datasets, tables, listings, and figures according to the project specifications as well as coordinating quality control efforts and implementing all programming required for study/project completion. Tasks • Generation and review of dataset specifications. Development and documentation of programs used to generate datasets generate listings, tables, and graphs; • Program validation includes the generation of validation documentation. Data preparation and documentation according to CDISC data standards. Design of integrated databases and development of mapping specifications for integrated datasets; • Preparation of electronic submission of clinical data.Intense and cross-functional interaction with other members of the project team. Perform all programming work by the SOPs.Providing internal consultancy in various review activities like database design, data validation rules, analysis plans, table shells, etc; • Interaction with clients. Design, development, documentation, and validation of tools and macros to continuously improve the quality and efficiency of processes applied. Writing of User Manuals; • Initial Training on existing processes, programs, etc. for new group members. Attending and representing the company at business conferences; • Monitoring resource needs, feeding back to programming management on the resource requirements of the study, timelines, ensuring that the internal and external deadlines are met. Implementation of study-specific efficiencies (example: study macros), including training of the programming team on their usage; • Ensuring that the project teams are working by study-specific requirements, as well as within the company’s SOPs, including ensuring that documentation and trackers are kept up to date. Coordination with other departments, such as biostatistics, data management, and project management; • Monitoring of study proposal assumptions and budgets, as well as flagging to project management if tasks outside the scope of the budget assumptions are identified; Requirements • BSc, MSc, or equivalent experience in information technology, mathematics, statistics, or life sciences; • Minimum of years of experience in processing and analyzing clinical trial data or demonstrated aptitude for statistical programming work; • Minimum of years of practical experience in the use of SAS concerning all aspects of software development; • Highly developed analytical skills, team player qualities (knowledge, skills, personal qualities); • Fluency in English; • Expert knowledge in SAS; • Knowledge of relevant regulatory requirements; • Knowledge of medical terminology and conduct and analysis of clinical trials; • Knowledge of different indications of clinical trials; • Knowledge of industry data standards (e.g. CDISC SDTM and ADaM); Interested? Join us Now