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Sr. Principal Statistics PAYS $93/HR Paramus, nj

Job

Global Channel Management, Inc.

Paramus, NJ (In Person)

$193,440 Salary, Full-Time

Posted 3 weeks ago (Updated 1 day ago) • Actively hiring

Expires 7/4/2026

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Job Description

Sr. Principal Statistics PAYS $93/HR Paramus, nj
Job Poster :
Global Channel Management, Inc.
Skills:
SAS Biostatistics |
Location:
Paramus , New Jersey ,
United States Of America Views:
256 Sr. Principal Statistics needs 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience Sr.
Principal Statistics requires:
    SAS, ICH
    guidelines, CDISC data structures, FDA guidelines, SAP preparation, TFL shells, CRF review, database design review, edit check specifications, sample size calculation, analysis dataset validation, CRO oversight
      Education:
      Ph.D. or MS in Statistics or Biostatistics
      • Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience
      • Excellent knowledge of SAS computer package
      • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines
      • Excellent organizational skills, time management, and ability to meet established deadlines.
      • Excellent communication and interpersonal skills to effectively interface with others
      • Exceptional interpersonal skills and problem-solving capabilities
      • Ability to work independently and collaboratively
      • Ability to provide leadership for the CRO statisticians and statistical programmers Sr.
      Principal Statistics duties:
      • Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
      • Review CRF, database design, and edit check specs
      • Review study quality surveillance plan and monitor study conduct
      • Prepare and/or review
      SAP, TFL
      shells and specifications for variable derivation
      • Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables
      • Provide statistical and validation support for statistical analysis, analysis datasets and TFL Review study report, manuscripts and other documents related to statistics
      • Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents
      • Perform other ad-hoc statistical activities as needed
      • Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming
      • Participates in monitoring CRO activities and reviewing CRO deliverables