Senior Biostatistician

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 NEEDED:

• 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

Regards,

Sukhpreet Basra

Clinical Recruiter “Talent Magnet”

Integrated Resources, Inc. 

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

Direct:732-429-1921 (Tel) 732-549-2030*241 | (F) 732-549-5549