Biostatistician

The Contract Biostatistician will be responsible for implementing and executing methodological and statistical aspects of clinical development programs. This position is open within Client's Rare Disease therapeutic area and provides the opportunity to contribute ongoing late phase studies as well as providing support on new and exciting clinical programs.

Qualification

Ph.D (M.S) in biostatistics or statistics with 3+ (5+) years of experience in a clinical trial setting (biotech, pharma, CRO, academic institution)

Excellent communication and writing skills including the ability to clearly describe advanced statistical techniques and interpret results

Thorough and up-to-date knowledge of advanced clinical trial statistical methodology, including time-to-event and recurrent event analysis, sequential methods, longitudinal data analysis (e.g. LME, GEE), techniques for handling missing data, nonparametric methods

Demonstrated productivity and ability to meet timelines for deliverables such as key results and final analyses

The ability to produce statistical documents such as publications or technical reports

Thorough and up-to-date working knowledge of SAS and additional statistical software (e.g. R, WinBUGS, etc.)

Understanding of clinical / regulatory concepts for at least one therapeutic area

With some supervision, ability to formulate statistical objectives, design and analyses for complex clinical projects

Good communication and developing negotiation skills

Ph.D (M.S) in biostatistics or statistics with 3+ (5+) years of experience in a clinical trial setting (biotech, pharma, CRO, academic institution)

Best Regards,

Anuj Mehta

973-967-3402