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