Statistical Programmer (AD/Director Level) - Contact

Location: Boston, MA (Hybrid – 2 days onsite/week)

Our client, an innovative biopharmaceutical company based in Boston, is seeking an experienced AD/Director Statistical Programmer to support critical statistical analyses for clinical programs, including regulatory submissions, safety monitoring, and clinical study reports (CSRs). This role offers the opportunity to make a significant impact within a growing Biostatistics & Biometrics team.

Key Responsibilities:

• Develop, validate, and maintain SAS programs for generating tables, listings, and figures (TLFs) from clinical trial data
• Perform QC checks and double programming for regulatory submissions (NDA/BLA)
• Provide statistical programming support for medical affairs initiatives, including publications and presentations
• Collaborate with biostatisticians to implement Statistical Analysis Plans (SAPs) and conduct ad-hoc analyses
• Leverage expertise with MediReal (or demonstrate the ability to learn it quickly)

Qualifications:

• 5–10 years of clinical SAS programming experience, ideally at the AD/Director level
• Proficiency in SAS (macros, Graph, STAT modules); familiarity with R or Python is a plus
• Prior experience supporting regulatory submissions (NDA/BLA, ISE/ISS)
• Bachelor’s degree in Computer Science, Statistics, or related field (or equivalent experience)

Work Arrangement & Compensation:

• Location: Boston, MA (Hybrid – 2 days onsite/week required for FTE)
• Compensation:
• Contract: $100/hour -$130/hr

Interested in making an impact on regulatory submissions for cutting-edge therapies? Apply now to learn more!