Senior Statistician

Katalyst HealthCares and Life Sciences

$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D or MS in Statistics or Biostatistics required.
  • 4+ years experience with Ph.D or 6+ years with MS in Pharmaceutical/CRO industry.
  • Strong proficiency with SAS software essential.
  • Solid understanding of ICH, CDISC, and FDA guidelines necessary.
  • Demonstrated organizational and time management skills required.
  • Excellent communication and interpersonal capabilities are a must.
  • Proven ability to lead CRO statisticians and programmers effectively.

Responsibilities

  • Review and prepare statistical protocol elements including sample size and analysis methods.
  • Oversee CRF, database layout, and edit check specifications.
  • Monitor quality and conduct of studies through surveillance plans.
  • Create and review SAP, TFL shells, and variable derivation specifications.
  • Collaborate with Statistical Programmers and Clinical Data Managers on data quality.
  • Support statistical analysis and datasets while validating outputs.
  • Actively participate in the preparation of study reports and manuscripts.
  • Respond to health authority inquiries with relevant statistical analyses and regulatory inputs.
  • Manage timelines and ensure effective collaboration across functions and with vendors.
  • Supervise CRO activities and assess their deliverables.

Benefits

  • Opportunities for continuing education and professional development.
  • Flexible working arrangements including remote work options.
  • Comprehensive health and wellness programs.
  • Supportive and collaborative team environment.
  • Engagement with cutting-edge clinical research initiatives.
Full Job Description
Job Description:
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.
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.
Requirements:
  • 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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