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Sr. Principal Statistics

Globalchannelmanagement

Paramus, New Jersey

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JOB DETAILS
SKILLS
Analysis Skills, Biostatistics, Biotech and Pharmaceutical, Case Report Form (CRF), Clinical Data Interchange Standards Consortium (CDISC), Clinical Data Management, Communication Skills, Contract Research Organization (CRO), Cross-Functional, Data Quality, Data Sets, Data Structures, Database Design, FDA (Food and Drug Administration), ICH Regulations, Identify Issues, Industry Standards, Interpersonal Skills, Leadership, Organizational Skills, Problem Solving Skills, SAP, Statistical Programming Languages, Statistics, Surveillance, Time Management
LOCATION
Paramus, New Jersey
POSTED
6 days ago

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

About the Company

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Globalchannelmanagement

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