Assoc Director, Statistical Programming

Scorpion Therapeutics; United States; Hybrid; USD 169,000 - 253,000; Full time

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

Associate Director, Statistical Programming (Hybrid; Foster City, CA or Raleigh, NC; NOT fully remote)

Job Responsibilities:

• Collaborate with Clinical Development to meet statistical analysis/reporting deliverables and timelines.
• Generate/oversee programming deliverables (tables, listings) for study reports and integrated summaries.
• Anticipate resource needs; ensure programming and documentation follow departmental procedures.
• Direct design/coding of analysis files; provide primary/secondary programming support and harmonize process-improvement initiatives.
• Apply strong communication skills; define and produce user-defined/ad hoc statistical reports with other departments.
• Anticipate and resolve study issues/conflicts; act as a key resource on multiple time-sensitive complex tasks.
• Create buy-in, negotiate timelines, manage critical deadlines, and lead programming-group strategic initiatives.

Basic Qualifications:

• BS (Biostatistics/Computer Science or equivalent) + 10+ years pharma/biotech experience
• OR MS + 8+ years
• OR PhD + 3+ years

Preferred Qualifications:

• 10+ years pharma/CRO experience; oncology/hematology/virology/inflammation experience; submission knowledge
• Pivotal studies + integrated analysis + regulatory submission activities
• SAS (including macros); CDISC (CDASH, SDTM, ADaM); GCP/ICH; complex fast-turnaround experience

Compensation/Benefits (if applicable):

Bay Area $195,670–$253,220; Raleigh $168,980–$218,680. May include annual bonus, stock incentives, paid time off, and medical/dental/vision/life insurance.