Sr Manager, Statistical Programming

Gilead Sciences

Base: $153,935.00 - $199,210.00; bonus/equity: dis...
Not specified
8+ years pharma/biotech experience
Advanced sas software proficiency
Cdisc standards knowledge (sdtm/adam)
Gilead Sciences is seeking a Senior Manager of Statistical Programming to contribute to the development of therapies for various diseases. The ideal candidate will have extensive experience in statistical programming within the pharmaceutical industry, particularly with regulatory submissions

Job Summary

  • The role involves collaborating with Clinical Development staff to ensure efficient production of analysis datasets and statistical outputs for study reports.
  • Candidates must have a thorough understanding of regulatory reporting requirements including electronic data submissions for FDA, PMDA, and EMA agencies.
  • Gilead offers a competitive salary range of $153,935.00 to $199,210.00 along with discretionary bonuses and comprehensive benefits packages.

Matching Summary

Match Score: 85

Gilead Sciences is seeking a Senior Manager of Statistical Programming to contribute to the development of therapies for various diseases. The ideal candidate will have extensive experience in statistical programming within the pharmaceutical industry, particularly with regulatory submissions.

Salary

Base: $153,935.00 - $199,210.00; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Medical, dental, vision, life insurance, and paid time off

Skills & Requirements

Must-have

  • 8+ years pharma/biotech experience
  • Advanced SAS software proficiency
  • CDISC standards knowledge (SDTM/ADaM)
  • Regulatory submission experience
  • Clinical trial design understanding

Nice-to-have

  • Oncology or virology domain expertise
  • Strong negotiation and communication skills
  • Experience with pivotal studies
  • Leadership and team management capabilities

Key Requirements

  • BS degree in Biostatistics/Computer Science with 8+ years experience
  • MS degree in Biostatistics/Computer Science with 4+ years experience
  • PhD degree in Biostatistics/Computer Sciences with 2+ years experience
  • Hands-on experience in pivotal studies and regulatory submissions
  • In-depth understanding of GCP and ICH regulatory requirements

Work Rights

Not specified

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