Senior Manager, Statistical Programming

Beam Therapeutics

Cambridge, MA, United States
Base: $155,000 - $190,000 usd; bonus/equity: not s...
On-site
Develop and maintain statistical programming functions
Manage cros and oversee programming activities
Generate analysis datasets, tables, listings, and figures
Beam Therapeutics is seeking a Senior Manager of Statistical Programming to lead and maintain programming functions for clinical studies and regulatory submissions. The candidate should possess extensive experience in pharmaceutical programming, particularly with SAS and CDISC standards, and demonstrate strong leadership and communication skills

Job Summary

  • The Senior Manager, Statistical Programming will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions.
  • Responsibilities include managing CROs, overseeing programming activities, generating analysis datasets, tables, listings, and figures, and performing ad hoc analysis.
  • The role requires advanced SAS programming skills, experience with CDISC (SDTM, ADaM), NDA or BLA submission experience, and the ability to build and mentor a team of programmers.

Matching Summary

Match Score: 85

Beam Therapeutics is seeking a Senior Manager of Statistical Programming to lead and maintain programming functions for clinical studies and regulatory submissions. The candidate should possess extensive experience in pharmaceutical programming, particularly with SAS and CDISC standards, and demonstrate strong leadership and communication skills.

Salary

Base: $155,000 - $190,000 USD; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Develop and maintain statistical programming functions
  • Manage CROs and oversee programming activities
  • Generate analysis datasets, tables, listings, and figures
  • Create CDISC SDTM and ADaM datasets
  • Utilize Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS, and R
  • Perform ad hoc analysis and review relevant documents

Nice-to-have

  • Advance a diversified portfolio of base editing programs
  • Contribute to a values-driven organization
  • Experience with R-Shiny is a plus

Key Requirements

  • MS or higher degree in Statistics, Mathematics, or related scientific Discipline
  • At least 10 years Pharmaceutical/Biotech programming experience
  • Advanced SAS programming skills and strong Statistical background
  • Experience and in-depth knowledge in CDISC including STDM, ADaM and controlled terminologies
  • NDA or BLA submission experience is required
  • Experience managing CROs and other data vendors
  • Knowledge of ICH guidelines, Good Clinical Practices, FDA / EMA / other regulatory authority guidance

Work Rights

Not specified

Tailored Resume

Cover Letter