Participation in budget preparation and resource planning within the project context
Supervision of external staff and service providers as well as training of internal teams when required
Ensuring timely and high-quality execution of all project tasks
Contribution to strategic direction under moderate supervision and within defined objectives
Support of CDISC-based e-submissions through the development, validation, and optimization of SAS macros and quality control programs
Application of statistical models and standardization of programming deliverables to address complex analytical requirements
this makes you so special to us:
Degree in Biostatistics, Computer Science, Pharmacy, or a comparable qualification
Experience in programming within the pharmaceutical industry or clinical research environment
Proficiency in CDISC standards and SAS programming
Knowledge of SDTM and ADaM
Communicative, effective, and results-oriented working style
Excellent command of both German and English
ep is a vision in which people, ideas and technology come together. We offer our employees and applicants the best career prospects - with an equal focus on both sides.
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