Senior Statistical Programming Lead

PTC Therapeutics; United States; On-site; USD 147,000 - 185,000; Full time

Benefits offered by this job

Short- and long-term incentives

Medical, dental, vision insurance

Retirement savings plans

Job summary

PTC Therapeutics, a global biopharmaceutical company, is seeking a Senior Statistical Programmer to lead the programming activities for clinical development studies and programs.

You will ensure timely analyses per protocols and SAPs, interact with CROs and study teams, review CRFs and derived datasets, and develop robust programming outputs.

This role offers collaboration across functions and opportunities to influence trial results and regulatory submissions.

Qualifications

• Master's degree in a quantitative science with 5+ years in stats or statistical programming.
• Proficiency in SAS (Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and databases.
• Experience with CDISC standards and drug development data analysis.

Responsibilities

• Lead statistical programming activities for clinical development studies and programs.
• Ensure timely analyses per protocols and SAPs, develop programs and outputs for trial reports.
• Collaborate with study teams and CROs, communicate statistical issues clearly.
• Review CRFs, CRF annotations, SAPs, TLGs, and related outputs.
• Interact with CROs to ensure analyses meet deliverables and resolve issues.
• Create/review derived dataset specifications and analysis datasets.
• May develop SOPs and training guidelines for statistical programming.
• Perform additional tasks as required by management.

Skills

SAS programming

R

CDISC

Communication skills

Independent work

Education

Master's degree in Statistics/Mathematics/CS

Tools

SAS

R

CDISC

Job description

PTC Therapeutics, a global biopharmaceutical company, is seeking a Senior Statistical Programmer to lead the programming activities for clinical development studies and programs.

You will ensure timely analyses per protocols and SAPs, interact with CROs and study teams, review CRFs and derived datasets, and develop robust programming outputs.

This role offers collaboration across functions and opportunities to influence trial results and regulatory submissions.