Statistics Opportunities at Parexel
By being hired into one of our Statistics Programming jobs at Parexel International, you’ll be a key member of the Parexel International team. Professionals in Statistics Programming careers come from a variety of backgrounds, bringing an assortment of knowledge and skills to every area of our business. A job in Statistics Programming at Parexel International may be waiting for you!
Statistical Programmer Senior/PrincipalJob ID 27739BR Shanghai, Shanghai Municipality, China
The Principal Biostatistician is expected to provide broad statistical support, contribute strategically to project decisions with a focus on pre-study planning, protocol development, sample size / power calculations, Statistical Analysis Plan preparation/ review, data quality reviews, development of tables / listings / figures, preparation / mapping of clinical study data for regulatory submission.
The Principal Biostatistician is expected to have an understanding of advanced statistical methods and to research complex and innovative statistical approaches (e.g, modeling and simulation, adaptive design / Bayesian statistics) and mentor junior staff in the use of these approaches.
The professional will participate in meetings and teleconferences and also provide consulting, interpretive and analytical support to Clients.
Review publications and clinical study reports. Assist with the technical details of client proposal documents.
Represent PAREXEL at client marketing and technical meetings.
QualificationsExperience in all tasks of a Trial Statistician.
Proven knowledge in Statistics and its applications to clinical trials.
Proven knowledge of statistical software packages.
Good communication and presentation skills.
Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability.
Excellent interpersonal, verbal and written communication skills.
Ability to identify and address issues proactively in a timely manner.
Ability to make appropriate decisions in ambiguous situations.
Carefully weighs the priority of project tasks and directs team accordingly.
Excellent computer literacy.
Demonstrate a sound knowledge of all relevant regulations, including GCP.
Good team player.
A master degree or equivalent in statistical science, mathematical analysis or related field plus 4 years relevant experience or a master’s degree plus 6 years relevant experience.
Comprehensive knowledge of statistical theory and methods and demonstrated ability to apply it to all phases of clinical trials.
Expertise in SAS programming including statistical analysis, data manipulation and scientific graphing.
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