What are the responsibilities and job description for the Statistical Programmer position at GQR?
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!
Salary : $100 - $130
