Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Regeneron

Associate Director, Statistical Programming – Pharmacometrics

Regeneron

Associate Director of Statistical Programming leading programming support for clinical studies at Regeneron. Providing project leadership, resource planning, and quality support for data analysis and reporting.

Posted 6/9/2026full-timeTarrytown • New Jersey, New York • 🇺🇸 United StatesSenior💰 $176,100 - $287,300 per yearWebsite

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Provide timely support to the study team on all programming matters
  • Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects
  • Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan
  • Provide programming support for all PMX deliverable in HAR request, data driven analysis, publications, conference
  • Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports

Requirements

What you’ll need
  • Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline
  • 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry
  • Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment
  • Understanding of relational database structure and reporting systems utilizing multiple data delivery applications
  • Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards
  • Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis)
  • Experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner
  • Mentor junior level staff in therapeutic area requirements
  • Develop collaborative work environment and be a positive role model.
  • Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python.
  • Good knowledges in AI use case in statistical programming and data sciences.

Benefits

Comp & perks
  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
SAS programmingrelational database structureCDISC data standardsbiostatisticspharmaceutical clinical developmentdata handlingPharmacokineticsimmunogenicityexposure response analysisstatistical programming
Soft Skills
project leadershipresource planningmentoringcollaborationpositive role model