Sr. Principal Statistics

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