Senior Programmer (m/f)

REFERENZNUMMER:

326461/11

IHRE AUFGABEN:

-Develop oncology generic programming code according to specifications, following internal guidelines, with high quality and within milestones
-Reinforce and implement programming standardization
-Enhance programming environment and systems
-Manage the testing of macros by setting and performing test scripts
-Establish standard processing procedures
-Write any documentation for standard macros uses (e.g. user manual)
-Maintain efficient interfaces with internal and external customers and communicate effectively across line functions
-Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities
-Provide input as required at all meetings, discussions and activities covering aspects of statistical reporting on trial level activities

IHRE QUALIFIKATIONEN:

-Proven experience using SAS in the analysis and the reporting of pharmaceutical data
-Working knowledge of database design/structures
-Extensive knowledge of SAS including Base, Macro, Stat, ODS etc
-Knowledge of CDISC data standards
-Profound experience in pharmaceutical SAS programming
-Experience in oncology therapeutic area
-Experience across all phases of trials and submissions
-Fluency English (oral and written)

WEITERE QUALIFIKATIONEN:

Biostatistician, Clinical data manager