Senior Bio statistician

Client: Direct Client

Location: Woodcliff Lake, NJ

Job Title: Senior Biostatistician 

Duration: 12 Months to 36 (Possible Extension)

Summary:

• 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.

Feel free to forward my email to your friends/colleagues who might be available

Education & Experience:

• 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

Warm Regards,

Jay Kaushik

Clinical Recruiter

Integrated Resources, Inc. 

IT Life Sciences Allied Healthcare CRO

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

(Direct) 732-429-1633 | (W) 732-549-2030 x 211 | (F) 732-549-5549

Linkedin: https://www.linkedin.com/in/jay-kaushik-a992a6a9?trk=hp-identity-name

Visit to our Website: www.irionline.com

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