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.
MSD

Assoc. Principal Scientist, Statistical Programming – Late-Stage, Infectious Disease

MSD

Statistical programming supporting late-stage drug and vaccine clinical development projects. Collaborating with stakeholders to ensure timely and high-quality deliverables.

Posted 5/27/2026full-timeNew Jersey, Pennsylvania • 🇺🇸 United StatesLead💰 $142,400 - $224,100 per yearWebsite

About the role

Key responsibilities & impact
  • supports statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects
  • development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures)
  • design and maintenance of statistical databases that support multiple stakeholder groups
  • assurance of deliverable quality and process compliance
  • development utilizing global and TA standards that optimize analysis and reporting
  • coordinating the activities of a global programming team
  • membership on departmental strategic initiative project teams

Requirements

What you’ll need
  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 or more years SAS programming experience in a clinical trial environment
  • Experience leading large and/or complex statistical programming projects that include coordinating the activities of a programming team
  • Broad knowledge and significant experience in developing analysis and reporting statistical programming deliverables using global and TA standards
  • Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise
  • Familiarity with statistical analysis methods and clinical data management concepts
  • US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level
  • Strong project management skills; A program leader; Determines appropriate programming methodology
  • Ability to comprehend statistical analysis plans which may describe statistical methodology to be programmed
  • Excellent communication and negotiation skills with a demonstrated history of teamwork and collaboration
  • Strategic thinking - ability to turn strategy into tactical activities
  • Experience in CDISC and ADaM standards

Benefits

Comp & perks
  • medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays, vacation, and compassionate and sick days

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 programmingstatistical analysisdata stepsproceduresSAS/MACROSAS/GRAPHclinical trial programmingstatistical programming deliverablesstatistical databasesCDISC
Soft Skills
project managementleadershipcommunicationnegotiationteamworkcollaborationstrategic thinkingprocess compliancequality assurancecoordination