Senior Biostatistician

Senior Biostatistician

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Senior Biostatistician Description:

• Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.

• 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; perform post-hoc statistical analyses as needed.

• Work with the project statistician and 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.

• Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, and ensure the quality of CRO deliverables.

• May work with the Health Outcome team on the design/analysis/validation of projects.

• May work on submission teams as a statistician and/or a programmer.

• Act as lead Statistician on complex trials and across multiple studies.

• Act as a lead representative of the of the biostatistics department on project teams.

Qualifications

• Must have a MS in Biostatistics/Statistics with at least 10-12 years of experience or a PhD in Biostatistics/ Statistics with at least 6 years of experience in the pharmaceutical, CRO or biotech industry.

• Strong SAS programming skills. – at least 3-5 years.

• Oncology experience is highly preferred.

• Good technical writing skills.

• Good communication skills (verbal and written).

• Strong teamwork ability/commitment and individual initiative.

• Strong organizational skills with ability to effectively manage multiple projects.

• We need is an experienced statistician who can do SAS programming at the same time can clearly interpret statistical concept and results to non-statisticians and key medical opinion leaders