Statistical Programmer
GQR
Job ID: li-4142281813
Location: Boston, MA
Description:
**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:**
* 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)
* **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!
Remote: False
Min Salary: 170000
Max Salary: 230000
Salary Frequency: yearly
Posted Date:
URL: https://www.linkedin.com/jobs/view/4142281813
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