Statistical Programming Lead — Associate Director (Hybrid)

Servier Pharmaceuticals; Boston (MA); Hybrid; USD 165,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision

Flexible time off

401(k)

Incentive programs

Job summary

Servier is seeking an Associate Director, Statistical Programming to lead programming activities across studies and assets. The role involves hands-on programming or oversight of outsourced deliverables, ensuring regulatory alignment and collaboration with statisticians and study teams.

You will mentor programmers, implement robust analysis processes, and ensure CDISC SDTM/ADaM compliance while coordinating with CROs and vendors to deliver timely, high-quality outputs for regulatory submissions.

Qualifications

• Masters in Statistics, Engineering or relevant field with 8+ years in statistical programming.
• Experience with SAS and CDISC ADaM/SDTM.
• Knowledge of regulatory submission guidelines.
• Strong study management and programming process expertise.
• Ability to lead and mentor statistical programmers.

Responsibilities

• Manage statistical programming deliverables across assets and oversee vendors.
• Oversee development and QC of analysis datasets and outputs for individual studies and integrated analyses.
• Ensure high-quality, traceable, timely outputs for regulatory needs.
• Mentor statistical programmers.
• Collaborate with statisticians and CROs to define analysis requirements.
• Ensure CDISC compliance of SDTMs and ADaMs.
• Forecast resource needs with portfolio programming lead.
• Plan and track project activities and timelines.

Skills

SAS programming

CDISC SDTM/ADaM knowledge

Regulatory knowledge

Project management

Mentoring

Communication skills

Education

Masters in Statistics, Engineering or relevant field

Tools

SAS

Job description

Servier is seeking an Associate Director, Statistical Programming to lead programming activities across studies and assets. The role involves hands-on programming or oversight of outsourced deliverables, ensuring regulatory alignment and collaboration with statisticians and study teams.

You will mentor programmers, implement robust analysis processes, and ensure CDISC SDTM/ADaM compliance while coordinating with CROs and vendors to deliver timely, high-quality outputs for regulatory submissions.