What are the responsibilities and job description for the Statistical Programmer position at GQR?
Statistical Programmer (AD / Director Level)
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 :
Work Arrangement & Compensation :
Interested in making an impact on regulatory submissions for cutting-edge therapies? Apply now to learn more!
Salary : $170,000 - $230,000
