Senior Manager, Statistical Programming — Lead Clinical Analyses (Hybrid)

PTC Therapeutics, Inc.; Warren Township (IA); On-site; USD 147,000 - 185,000; Full time

Benefits offered by this job

Travel up to 20%

Job summary

PTC Therapeutics, Inc. is seeking a Senior Manager, Statistical Programming to lead programming for clinical development studies, collaborating with CROs and internal biostatistics teams. The role involves ensuring timely analyses and contributing to the generation of integrated trial results.

You will oversee data handling and reporting alongside cross-functional partners in a dynamic, global environment. The position requires a Master’s degree in a quantitative science and at least 5 years of

Qualifications

• Master’s degree in a quantitative science and 5+ years of experience in statistics or statistical programming in pharma/CRO.
• Proficiency in SAS (Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and working knowledge of R.
• CDISC experience and knowledge of clinical data analysis and reporting in drug development.

Responsibilities

• Lead the statistical programming activities for assigned clinical development studies and programs.
• Ensure timely statistical analyses of clinical data per protocols and SAPs, via direct work or CRO oversight.
• Participate in study team meetings as a Biostatistics resource and communicate statistical issues.
• Assist in CRO assessment, selection and evaluation.
• Review CRFs, annotations, SAPs, TLGs and related artifacts.
• Create/review derived dataset specifications and analysis datasets.
• Develop SOPs and training guidelines related to statistical programming.
• Perform other tasks as needed by management.

Skills

SAS programming

SAS macros

SAS/Stat

SAS/Graph

ODS

R

CDISC

Communication

Independent work

Analytical thinking

Time management

Education

Master’s degree in quantitative science

Tools

Base SAS

SAS/Graph

SAS/macros

DB systems

Job description

PTC Therapeutics, Inc. is seeking a Senior Manager, Statistical Programming to lead programming for clinical development studies, collaborating with CROs and internal biostatistics teams. The role involves ensuring timely analyses and contributing to the generation of integrated trial results.

You will oversee data handling and reporting alongside cross-functional partners in a dynamic, global environment. The position requires a Master’s degree in a quantitative science and at least 5 years of