IT Elite Inc is looking for Statistician to work on a long term client project.

Full time, W-2 Opportunity. Long Term and No Corp to Corp.

Qualifications required:

• PhD or Master’s degree in a related field
• 8+ years working in clinical trials with at least 3 years working in a CRO environment.
• 5+ years of leading Biostatisticians or cross-functional teams.
• Clinical trial designs in Phase I – IV studies, with experience in Adaptive or Group Sequential designs a plus.
• Thorough understanding of statistical principles.
• Experienced in SAS programming, and knowledge of SAS procedures and other statistical software (i.e. R, EAST)
• Submissions experience preferred.
• Experience presenting to the DMC, blinded and un-blinded results
Adept in CDISC ADaM / SDTM standards, with experience in the generation of ADaM specifications and QC of datasets strongly desired.
• Excellent communication and organizational skills.

Statistical responsibilities include:

• participating in the development of study protocols, including participation in study design discussions and sample size calculations;
• developing statistical analysis plans (SAPs), including analysis data and TLG specifications;
• performing statistical analysis;
• interpreting statistical results;
• preparing final analyses and outputs, including integrated summaries for submissions

Responsibilities include:

• performing general project management;
• supporting business development for new project work;
• utilizing your strong communication skills to present and explain methodology and consequences of decisions in lay terms;
• mentoring statisticians that may be new to certain types of studies and/or therapeutic areas;
• leading by example, as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
• being adaptable and flexible when priorities change

If your skills match the above requirement, Please forward your resume as a word attachment with salary requirement and contact information.