Hybrid Associate Director, Statistical Programming - Lead

Scorpion Therapeutics

United States

Hybrid

USD 169,000 - 253,000

Full time

14 days+

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Benefits offered by this job

Stock incentives
Paid time off
Medical/dental/vision/Life insurance

Job summary

Scorpion Therapeutics seeks an Associate Director of Statistical Programming for a hybrid role based in Foster City, CA or Raleigh, NC. You will collaborate with Clinical Development to meet analysis deliverables, generate tables/listings for study reports, and oversee programming deliverables while driving process improvements.

Strong SAS/CDISC experience and regulatory submission knowledge are required. Ideal candidates have a PhD/MS/BS with extensive pharma/biotech experience and demonstrated

Qualifications

  • BS/MS/PhD in a relevant field with pharma/biotech experience.
  • Experience with SAS, CDISC standards and regulatory submissions.
  • Strong programming leadership and cross-functional collaboration.

Responsibilities

  • Collaborate with Clinical Development to meet analysis and reporting timelines.
  • Generate/oversee tables and listings for study reports and integrated summaries.
  • Direct design/coding of analysis files and harmonize processes.
  • Provide primary/secondary programming support and implement improvements.
  • Communicate findings and deliver ad hoc reports with other teams.
  • Lead programming-group initiatives and manage deadlines.

Skills

SAS
CDISC
GCP/ICH
Biostatistics

Education

BS in Biostatistics/CS
MS in Biostatistics/CS
PhD in relevant field

Tools

SAS macros
CDASH
SDTM
ADaM

Job description

Scorpion Therapeutics seeks an Associate Director of Statistical Programming for a hybrid role based in Foster City, CA or Raleigh, NC. You will collaborate with Clinical Development to meet analysis deliverables, generate tables/listings for study reports, and oversee programming deliverables while driving process improvements.

Strong SAS/CDISC experience and regulatory submission knowledge are required. Ideal candidates have a PhD/MS/BS with extensive pharma/biotech experience and demonstrated

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