Strategic Leader, Clinical Statistical Programming

PTC Therapeutics, Inc; New Jersey; Hybrid; USD 147,000 - 185,000; Full time

Benefits offered by this job

Short- and long-term incentives

Medical plan

Dental plan

Vision plan

Retirement savings plan

Job summary

PTC Therapeutics, Inc. is a global biopharmaceutical company seeking a Senior Manager, Statistical Programming to lead programming for clinical studies and partner with CROs. The role emphasizes SAS-based analyses, CDISC standards, and collaboration across functional teams.

The position requires a Master’s degree in a quantitative field and at least 5 years of statistics/programming experience in pharma/CRO environments, with strong communication and problem-solving skills.

Qualifications

• Master's degree in a quantitative science (e.g., Statistics, Mathematics, Computer Science) and 5+ years in statistics or statistical programming in pharma/CRO setting.

Responsibilities

• Lead statistical programming activities for clinical development studies and programs.
• Ensure timely analyses per protocols and SAPs; develop statistical programs and output for integrated reports.
• Serve as the statistics/programming resource in study team meetings and CRO oversight.
• Assess, select and evaluate CROs; interact with CROs for data analysis.
• Review CRFs, CRF annotations, Statistical Analysis Plans, and related outputs.
• Create/review derived dataset specifications and analysis datasets.
• Possibly develop SOPs and training guidelines for statistical programming.

Skills

SAS programming

CDISC

R programming

Statistical analysis

Communication

Independent work

Cross-functional teamwork

Education

Master's degree in quantitative science

Tools

SAS

R

Job description

PTC Therapeutics, Inc. is a global biopharmaceutical company seeking a Senior Manager, Statistical Programming to lead programming for clinical studies and partner with CROs. The role emphasizes SAS-based analyses, CDISC standards, and collaboration across functional teams.

The position requires a Master’s degree in a quantitative field and at least 5 years of statistics/programming experience in pharma/CRO environments, with strong communication and problem-solving skills.