Hi Partners Hope you are doing great.
*Duration: They are all 1 year contracts with possibilities for extension in 6 month increments until worker reaches tenure at the 3 year mark.* *Biostat Programmer – 2 openings * Oncology PCU Qualifications and education required: • Minimum of Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related science discipline. Masters preferred. Experience required: • Minimum 3 years’ experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 6+ years’ experience preferred. • Some project experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment. Skills and aptitude required: • Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Knowledge of SDTM and ADaM standards. • Proven experience with UNIX and Windows operating systems. • Understanding of the software development life cycle. • Understanding of FDA guidelines. • Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. • Applies good judgment and demonstrates initiative to resolve issues. • Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment, managing that team as required NOTE: EDUCATION REQUIREMENTS: Minimum of Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related science discipline. Masters preferred. DOMESTIC SCHOOLS PREFERRED. PHARMA INDUSTRY NOT CRO. STABLE WORK HISTORY ---------------------------------------------------------------------------------- *Biostatistician– 1 opening * Under the guidance of lead project statistician • Develop statistics model and perform simulation to optimize study design and analysis. . Work with the clinical study team on study design, development and/or review of clinical study protocols. • Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; • Work with clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality. • perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, and ensure the quality of deliverables. Perform post-hoc statistical analyses as needed. • Generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies *QUALIFICATIONS NEEDED:* • Must have a PhD in Biostatistics/ Statistics with knowledge of drug development. • Strong SAS programming skills. Hands on experience in statistics model simulation • Good communication skills (verbal and written). • Ability to effectively work on multiple projects Thanks Chetan Ghediya CyberThink Inc [email protected] 732-481-4174 Ext- 6647 -- You received this message because you are subscribed to the Google Groups "US_IT.Groups" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/us_itgroups. For more options, visit https://groups.google.com/d/optout.
