Senior Principal Statistical Programmer

Katalyst HealthCares and Life Sciences

$110K — $140K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D or MS in Statistics or Biostatistics
  • 4+ years (Ph.D) or 6+ years (MS) of experience in Pharmaceutical/CRO industry
  • Proficient in SAS software
  • Strong understanding of ICH guidelines and CDISC data structures
  • Excellent organizational and time management skills
  • Strong communication and interpersonal abilities
  • Ability to lead CRO statisticians and programmers

Responsibilities

  • Review protocols and prepare statistical sections
  • Design study elements including sample size calculations and analysis methods
  • Monitor study quality and conduct
  • Prepare and review SAP, TFL shells, and variable derivation specs
  • Identify data quality issues with Statistical Programmers and Clinical Data Manager
  • Provide statistical support for analysis datasets and TFL
  • Review study reports, manuscripts, and regulatory documents
  • Engage in responses to health authorities and new analyses as required
  • Oversee CRO activities and review deliverables

Benefits

  • Comprehensive health insurance
  • Retirement plan with company match
  • Generous paid time off policy
  • Flexible work schedule
  • Professional development opportunities
Full Job Description
Summary of Position:
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.

Duties and Responsibilities:
  • 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
  • Other duties as assigned
Must have:
  • 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
  • bility to work independently and problem-solve
  • bility to provide leadership for the CRO statisticians and statistical programmers

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