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: 510 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) Bachelors 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) Employment Type: Open to contract, contract-to-permanent, or permanent roles Compensation: Contract: $100/hour Permanent: $170,000$230,000 base Interested in making an impact on regulatory submissions for cutting-edge therapies? Apply now to learn more! GQR
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