Lead Statistical Programmer — Remote (CDISC, Clinical Data)

Servier Pharmaceuticals; Boston (MA); Hybrid; USD 151,000 - 172,000; Full time

Benefits offered by this job

Hybrid work option

Competitive benefits

Job summary

Servier is seeking a Sr Manager, Statistical Programming in Boston to lead study-level programming efforts, ensuring regulatory alignment and high-quality deliverables. You will supervise programming activities, guide outsourced work, and collaborate with statisticians and CRO programmers.

The role requires a Masters in Statistics or related field with ≥5 years in clinical programming, with SAS expertise and strong CDISC SDTM/ADaM knowledge.

Qualifications

• Masters in Statistics, Engineering, or relevant field with at least 5 years of experience in statistical programming or biostatistics in the Pharmaceutical/Biotechnology industry.
• Clinical Development experience preferred
• Experience with statistical programming in Oncology desirable
• Strong knowledge of CDISC ADaM and SDTM

Responsibilities

• Provide programming support for the development or QC of SDTMs, ADaM specifications, ADaM datasets, and TLFs.
• Manage statistical programming activities for a clinical study related to CSR, iDMC, adhoc analysis and publications etc.
• Ensure high quality, traceability, reproducibility, and timeliness of statistical programming deliverables to meet regulatory requirements.
• Independently implement routine and non-standard analysis algorithms for assigned projects or studies.
• Collaborate with statisticians, CRO programmers to define and implement analysis requirements and perform sponsor oversight.
• Deliver exemplary performance and solve complex technical problems to inspire other programmers.

Skills

Statistical programming

Project management

Team leadership

Communication

Education

Masters in Statistics or related field

Tools

SAS

CDISC SDTM

CDISC ADaM

Job description

Servier is seeking a Sr Manager, Statistical Programming in Boston to lead study-level programming efforts, ensuring regulatory alignment and high-quality deliverables. You will supervise programming activities, guide outsourced work, and collaborate with statisticians and CRO programmers.

The role requires a Masters in Statistics or related field with ≥5 years in clinical programming, with SAS expertise and strong CDISC SDTM/ADaM knowledge.