Director, Statistical Programming

Definium Therapeutics

Completely RemoteFull TimeHealthcare & Telemedicine
Posted Today

Job description

Responsibilities

  • Manage a group of statistical programmers to provide programming support for assigned projects from datasets creation to data analysis
  • Serve as lead statistical programmer for regulatory filing teams to support integrated data analyses
  • Deliver high quality SDTM and ADaM datasets meeting CDISC standards
  • Deliver high quality integrated databases to support safety and efficacy analyses
  • Produce high quality DEFINE packages for SDTM and ADaM
  • Manage vendor deliverables regarding quality, timeline, and budget in collaboration with biostatisticians
  • Perform statistical data analysis and independent validation using SAS programs
  • Participate in developing SOPs and processes for statistical programming activities

Requirements

  • Master's Degree in Biostatistics, Statistics, Computer Science, or a relevant field
  • At least 15 years of experience in statistical programming for clinical trial data in pharma, biotech, or CRO environments
  • Proven experience building and leading statistical programming groups
  • Deep understanding of data standards and creating DEFINE packages for regulatory filing
  • Proficiency in SAS, including complex data steps, macro languages, and analysis procedures (PROC Freq, REPORT, GLM, MIXED)
  • Extensive experience in statistical vendor management
  • Strong organizational, project, and resource management skills

Preferred Qualifications

  • Experience providing statistical programming support for CNS clinical trials
  • Experience providing statistical programming support for regulatory filing

Benefits

  • 100% paid health benefits including Medical, Dental, and Vision for employees and dependents
  • 401(k) program with company match
  • Flexible time off
  • Generous parental leave

About the Company

Definium Therapeutics is a late-stage clinical biopharmaceutical company focused on applying scientific rigor to psychedelics to develop accessible treatments for psychiatric and neurological disorders.

Skills & tools

SASCDISCSDTMADAM

What the team is looking for

Use this list as a quick fit check before you apply.

  1. 01Master's Degree in Biostatistics, Statistics, or Computer Science
  2. 0215+ years of clinical trial statistical programming experience
  3. 03Expertise in SAS and CDISC standards
  4. 04Experience leading statistical programming teams
  5. 05Experience managing statistical vendors
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