SVP, Biometrics & Oncology Data Strategy

Erasca, Inc.

Northern, San Diego (KY, CA)

Hybrid

USD 350,000 - 415,000

Full time

7 days ago
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Benefits offered by this job

Paid Time Off
Medical Insurance
Dental Insurance
Vision Insurance
401(k) Plan
Employee Stock Purchase Program
Pet Insurance
Disability Insurance
Flexible Spending Accounts
Life/AD&D

Job summary

Erasca, Inc. is seeking a Senior Vice President of Biometrics to lead Biostatistics, Statistical Programming & Analysis, and Clinical Data Management from IND-enabling through registration and launch.

This role combines executive leadership with hands-on execution and cross-functional collaboration. The ideal candidate has 15+ years in pharma/biotech biometrics, a PhD in statistics/biostatistics, and a proven track record in oncology drug development and regulatory interactions, with strong

Qualifications

  • Minimum of 15 years relevant experience in pharma/biotech, large and small companies.
  • PhD in statistics or biostatistics required.
  • Experience in oncology drug development and regulatory interactions.

Responsibilities

  • Build, lead, and mentor Biostatistics, Statistical Programming & Analysis, and Clinical Data Management teams.
  • Ensure data design, analysis, and submission datasets meet regulatory requirements.
  • Provide biometrics expertise to senior management and clinical teams.
  • Contribute to study protocols, reports, INDs, NDAs, and labeling.
  • Represent biometrics in regulatory interactions and with health authorities.
  • Stay abreast of new statistical methods and biometrics SOPs.

Skills

Biostatistics
Leadership
SAS
CDISC
Regulatory
ICH/FDA
Statistical programming
Team mentoring
Communication

Education

PhD in Biostatistics

Tools

SAS
R

Job description

Erasca, Inc. is seeking a Senior Vice President of Biometrics to lead Biostatistics, Statistical Programming & Analysis, and Clinical Data Management from IND-enabling through registration and launch.

This role combines executive leadership with hands-on execution and cross-functional collaboration. The ideal candidate has 15+ years in pharma/biotech biometrics, a PhD in statistics/biostatistics, and a proven track record in oncology drug development and regulatory interactions, with strong

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