- Extensive experiences in phase III trials, in particular, CV trials, for example familiar with statistical analysis plan, clinical study report, database, analysis data sets and statistical programming specification
- Experiences in worldwide submission, in particular, PMDA in Japan – providing statistical analysis for ad hoc requests
- Strong statistical training, in particular, survival analysis
- Leadership (establish priorities and objectives, implement actions and plans and always look for solutions independently)
- Proactive communication with project team members
- Motivated
- At least 5 years of pharmaceutical experience at Ph.D. level (or 8 years at MS level ) in biostatistics, statistics and epidemiology
- Excellent communication skills (verbal and written)
- Good team player
- Advanced level in SAS
- Located in Raritan
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